Fresh Recalls

Latest recalls

Browse the most recent U.S. safety recalls in our connected official government data.

2,490 recalls are currently indexed. Showing the 100 most recent.

CPSC · Bicycles & Accessories · September 3, 2026

MONDRAKER USA Recalls Mountain Bicycles Equipped with ONOFF S9 Carbon MTB Handlebars Due to Risk of Serious Injury or Death from Fall Hazard

The affected handlebars may crack or fracture during use, which can lead to loss of control, posing a risk of serious injury or death from fall hazard.

Company / brand: MONDRAKER USA

Official ID 26746 · Official notice ↗

CPSC · Cleaners/Cleaning Products · September 3, 2026

Clorox Puerto Rico Recalls 6 Million Scented Mistolin and Lestoil Multi-Purpose Cleaners Due to Risk of Exposure to Bacteria

The recalled products may contain bacteria, including Pseudomonas aeruginosa, which is an environmental organism found widely in soil and water. People with weakened immune systems…

Company / brand: Clorox Manufacturing Company of Puerto Rico

Official ID 26741 · Official notice ↗

CPSC · Adapter/Power Supply/Charger/Battery · September 3, 2026

Truststone Group Recalls XO Poppy Power Trip Magnetic Wireless Power Banks Due to Fire and Burn Hazards; Sold Exclusively at TJX and Marshalls Stores

The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers.

Company / brand: Truststone Group of New York

Official ID 26740 · Official notice ↗

CPSC · Toys · September 3, 2026

Skip Hop Recalls Baby Sesame Street Elmo Silicone Teethers Due to Risk of Serious Injury or Death from Choking Hazard

The black eyes can detach from the recalled teether if frozen, posing a risk of serious injury or death from a choking hazard.

Company / brand: The William Carter Company

Official ID 26739 · Official notice ↗

CPSC · Squeeze Or Squeaker Toys · September 3, 2026

GIHNJSI Squeezy Dumplings Toys Recalled Due to Serious Ingestion, Choking and Obstruction Hazards; Sold on Amazon by Chenyuanhui

The squeezy toys contain water beads. If ingested, water beads expand and can pose deadly ingestion, choking, and intestinal obstruction hazards inside a child’s body, resulting in…

Company / brand: Xiamen Liuhui Electric Technology Co

Official ID 26738 · Official notice ↗

CPSC · Squeeze Or Squeaker Toys · September 3, 2026

OKK Trading Recalls Rainbow Mystery Squishy Bun Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys

The squishy bun toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a deadly ingestion hazard. If …

Company / brand: OKK Trading

Official ID 26737 · Official notice ↗

CPSC · Desks, Dressers, Chests, Bureaus, Or Buffets · September 3, 2026

Gizoon Direct Recalls Six-Drawer Double Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. T…

Company / brand: Airiva

Official ID 26736 · Official notice ↗

CPSC · Chairs, Not Specified · September 3, 2026

Branch Recalls Ergonomic Chairs Due to Fall Hazard

The backrests of the chairs can detach, posing a fall hazard to consumers.

Company / brand: Bureau Office

Official ID 26735 · Official notice ↗

CPSC · Air Conditioners · September 3, 2026

Daikin Comfort Technologies Manufacturing Recalls Amana Through-The-Wall Air Conditioners and Heat Pumps Due to Risk of Serious Injury from Fire

The snubber circuit can emit flames if it shorts, posing a risk of serious injury due to fire hazard.

Company / brand: Daikin Comfort Technologies Manufacturing

Official ID 26734 · Official notice ↗

CPSC · Adult Bed Rails · September 3, 2026

Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Loyoda Direct and Loyoda

The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of th…

Company / brand: Fangzhou Overseas Consulting Shenzhen Co

Official ID 26733 · Official notice ↗

CPSC · Toys & Children · September 3, 2026

SHEIN Distribution Corporation Recalls Spiral Toys Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Ball Ban

The toys violate the small ball ban because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.

Company / brand: SHEIN Distribution of Los Angeles

Official ID 26732 · Official notice ↗

CPSC · Speakers · September 3, 2026

Audio Partnership Recalls Cambridge Audio Yoyo (M) Portable Bluetooth Speakers Due to Fire Hazard

The lithium-ion batteries in the Cambridge Audio Yoyo (M) Portable Bluetooth Speaker can overheat, posing a fire hazard.

Company / brand: Audio Partnership

Official ID 26731 · Official notice ↗

CPSC · Desks, Dressers, Chests, Bureaus, Or Buffets · September 3, 2026

Nanjing Wu Hai Smart Home Appliance Store Recalls Alanca 6-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. T…

Company / brand: Nanjing Wu Hai Smart Home Appliance Store

Official ID 26730 · Official notice ↗

NHTSA · Vehicle · September 1, 2026

Peterbilt 548 recall (26V567000)

Delayed brake response time can increase the risk of a crash.

Company / brand: Paccar Incorporated

Official ID 26V567000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Forest River Bus Equipment Adaptive/Mobility recall (26V565000)

A wheelchair lift that continues to move while occupied increases the risk of injury.

Company / brand: Forest River Bus

Official ID 26V565000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Light Boy GBX12SK recall (26V564000)

A detach light tower can become a road hazard for other vehicles, increasing the risk of a crash or injury.

Company / brand: Light Boy America

Official ID 26V564000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Forest River Vibe recall (26V563000)

Unvented exhaust fumes increase the risk of injury from carbon monoxide poisoning.

Company / brand: Forest River

Official ID 26V563000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Chrysler Suspension recall (26V562000)

Rear coil springs that detach from the vehicle while driving increase the risk of a crash.

Company / brand: Chrysler

Official ID 26V562000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Chrysler Electronic Stability Control (Esc) recall (26V561000)

A loss of electronic stability control increases the risk of a crash.

Company / brand: Chrysler

Official ID 26V561000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Ram 1500 recall (26V560000)

A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.

Company / brand: Chrysler

Official ID 26V560000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Tesla Model Y recall (26V558000)

A lateral link separation could shift the wheel alignment, causing a loss of vehicle control and increasing the risk of a crash.

Company / brand: Tesla

Official ID 26V558000 · Official record ↗

NHTSA · Vehicle · August 31, 2026

Tiffin Wayfarer recall (26V557000)

LP tanks that cannot be shut off increase the risk of a fire. Additionally a loose LP tank may detach and become a road hazard, increasing the risk of a crash.

Company / brand: Tiffin Motorhomes

Official ID 26V557000 · Official record ↗

NHTSA · Vehicle · August 31, 2026

Blue Bird Vision School Bus recall (26V556000)

A wheelchair lift that continues to move while occupied increases the risk of injury.

Company / brand: Blue Bird Body Company

Official ID 26V556000 · Official record ↗

NHTSA · Vehicle · August 31, 2026

Jayco Electrical System recall (26V555000)

The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.

Company / brand: Jayco

Official ID 26V555000 · Official record ↗

NHTSA · Vehicle · August 31, 2026

Jayco Equipment recall (26V554000)

Incorrect information may result in the wrong sized replacement tires being installed, increasing the risk of a crash.

Company / brand: Jayco

Official ID 26V554000 · Official record ↗

NHTSA · Vehicle · August 28, 2026

Magic Tilt Aluminum Watercraft Trailer recall (26V553000)

A detached winch may increase the risk of injury to people near the trailer.

Company / brand: Magic Tilt Trailers

Official ID 26V553000 · Official record ↗

NHTSA · Vehicle · August 28, 2026

Heartland Bighorn recall (26V552000)

Referencing the incorrect weight could result in the trailer being overloaded, increasing the risk of a crash.

Company / brand: Jayco

Official ID 26V552000 · Official record ↗

NHTSA · Vehicle · August 27, 2026

Altec Service Body recall (26V551000)

An electrical short-circuit can increase the risk of a fire.

Company / brand: Altec Industries

Official ID 26V551000 · Official record ↗

CPSC · Toys · August 27, 2026

Montessori Baby Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Chillife Official

The recalled baby toy sets contain a pull string teething toy that violates the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The …

Company / brand: Shenzhenshixingchuangyiyimaoyouxiangongsi (Shenzhen Xingchuangyi Trading Co

Official ID 26727 · Official notice ↗

CPSC · Desks, Dressers, Chests, Bureaus, Or Buffets · August 27, 2026

Walmart Reannounces Recall of Mainstays Nine-Drawer Fabric Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Walmart Distributed Recalled Dressers Post-Recall; Sold to Consumers Through Liquidators

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or death to children. Th…

Company / brand: Hop Thang Interior Wood Co

Official ID 26726 · Official notice ↗

CPSC · Pressure Washers · August 27, 2026

Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Sold on Amazon by YERYORK

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing serious risks of injury or death from shock and ele…

Company / brand: Lanzhou Xinshi Mingchen Information Technology Co

Official ID 26725 · Official notice ↗

CPSC · Clothing · August 27, 2026

Little Loves & Co. Recalls Youth Clothing with Drawstrings Due to Risk of Serious Injury or Death from Entrapment Hazard

The drawstrings in the recalled clothing can get caught on objects and cause death or serious injury to children due to an entrapment hazard.

Company / brand: Little Loves & Co

Official ID 26724 · Official notice ↗

CPSC · Pressure Washers · August 27, 2026

Steelite Pressure Washers Recalled Due to Risk of Serious Injury or Death from Shock and Electrocution Hazards; Sold on Amazon by Longer 3D

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing a risk of serious injury or death from shock and el…

Company / brand: Longer Technology (Hong Kong)

Official ID 26723 · Official notice ↗

CPSC · Lights & Accessories · August 27, 2026

Excel Industries Recalls Accessory LED Light Kits Due to Risk of Serious Injury from Fire Hazard

The light bars can overheat or produce flames, posing a risk of serious injury from a fire hazard.

Company / brand: Excel Industries

Official ID 26722 · Official notice ↗

CPSC · Baby Walkers Or Jumpers · August 27, 2026

Kmaier Recalls Infant Walkers Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers

The recalled walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a deadly fall …

Company / brand: FENUN

Official ID 26721 · Official notice ↗

CPSC · Hi-Fi And Stereo Equip., Amplifiers, Speakers · August 27, 2026

AudioLineOut Recalls Studio Six Headphone Amplifiers Due to Risk of Serious Injury or Death from Electrocution Hazard

When the amplifiers are used with aftermarket metal base tubes, the bare metal can become electrified, posing a risk of serious injury or death from electrocution.

Company / brand: AudioLineOut

Official ID 26720 · Official notice ↗

CPSC · Toys · August 27, 2026

HABA USA Recalls Rainbow Rattle Grasping and Teething Toys Due to Risk of Serious Injury or Death from Choking and Ingestion Hazards

The glued knot on the elastic cord can become untied on the recalled product, allowing young children access to the small wooden and plastic pieces, posing a risk of serious injury…

Company / brand: Habermaass

Official ID 26719 · Official notice ↗

CPSC · Towels Or Cloths · August 27, 2026

Diamond Wipes International Recalls MD Wipe Outz Numbing Tattoo Wipes Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging

The recalled numbing wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging of the wipes is not chil…

Company / brand: Diamond Wipes International

Official ID 26718 · Official notice ↗

CPSC · Cleaning Equipment, Inc. Brooms, Mops, Brushes, Etc · August 27, 2026

Conair Expands Recall of Cuisinart Grill Brushes Due to Ingestion Hazard; Over 3.6 Million Brushes Now Recalled

Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.

Company / brand: Conair of Stamford

Official ID 26717 · Official notice ↗

NHTSA · Vehicle equipment · August 26, 2026

Bell Sports recall (26E061000)

A helmet that does not provide adequate impact protection increases the risk of injury in a crash.

Company / brand: Bell Sports

Official ID 26E061000 · Official record ↗

NHTSA · Vehicle · August 25, 2026

Ford Motor Company Structure recall (26V550000)

Improperly tightened vehicle joints may lead to a loss of vehicle control, electrical failure, or detached parts, increasing the risk of a crash or fire.

Company / brand: Ford Motor Company

Official ID 26V550000 · Official record ↗

NHTSA · Vehicle · August 25, 2026

Mitsubishi Motors North America Back Over Prevention recall (26V549000)

A rearview image that does not display properly reduces the driver's view behind the vehicle, increasing the risk of a crash.

Company / brand: Mitsubishi Motors North America

Official ID 26V549000 · Official record ↗

NHTSA · Vehicle · August 25, 2026

Ford Motor Company Engine And Engine Cooling recall (26V548000)

An unexpected loss of drive power increases the risk of a crash.

Company / brand: Ford Motor Company

Official ID 26V548000 · Official record ↗

NHTSA · Vehicle · August 25, 2026

Ford Mustang recall (26V547000)

A loss of driver power increases the risk of a crash. In addition, a loss of headlight function or windshield washing system function can reduce visibility, increasing the risk of …

Company / brand: Ford Motor Company

Official ID 26V547000 · Official record ↗

NHTSA · Vehicle · August 24, 2026

Daimler Trucks North America Structure recall (26V546000)

A seat belt anchor with a missing connector plate may fail to properly restrain the driver and insufficient joint strength may not adequately protect passengers, increasing the ris…

Company / brand: Daimler Trucks North America

Official ID 26V546000 · Official record ↗

NHTSA · Vehicle equipment · August 24, 2026

Rennline Lower Control Arm recall (26E060000)

A damaged subframe my lead to a loss of steering control, increasing the risk of a crash.

Company / brand: Rennline Automotive

Official ID 26E060000 · Official record ↗

NHTSA · Vehicle · August 21, 2026

Kia Ev9 recall (26V545000)

A child in the front seat may be at a greater risk of injury if the air bag deploys during a crash.

Company / brand: Kia America

Official ID 26V545000 · Official record ↗

NHTSA · Vehicle · August 21, 2026

Paccar Incorporated Seats recall (26V544000)

A short circuit increases the risk of a fire.

Company / brand: Paccar Incorporated

Official ID 26V544000 · Official record ↗

NHTSA · Vehicle · August 21, 2026

Cornell Pump Company Structure recall (26V543000)

Instability while towing increases the risk of a crash.

Company / brand: Cornell Pump Company

Official ID 26V543000 · Official record ↗

NHTSA · Vehicle · August 21, 2026

Altec Industries Forward Collision Avoidance recall (26V541000)

An improperly calibrated system may have a delayed braking response, increasing the risk of a crash.

Company / brand: Altec Industries

Official ID 26V541000 · Official record ↗

NHTSA · Vehicle · August 20, 2026

Ford F-650 SD recall (26V568000)

A liftgate that falls unexpectedly increases the risk of injury.

Company / brand: Marathon Industries

Official ID 26V568000 · Official record ↗

NHTSA · Vehicle · August 20, 2026

Lucid Air recall (26V540000)

An overheated circuit increases the risk of a fire. A loss of the center brake light or front lights can also decrease visibility, increasing the risk of a crash.

Company / brand: Lucid Usa

Official ID 26V540000 · Official record ↗

NHTSA · Vehicle · August 20, 2026

Rossmonster Vans Equipment recall (26V538000)

An overheated printed circuit board increases the risk of a fire.

Company / brand: Rossmonster Vans

Official ID 26V538000 · Official record ↗

NHTSA · Child car seat · August 20, 2026

Britax Child Safety Child Seat recall (26C006000)

A child may fall after a partial detachment, increasing the risk of injury.

Company / brand: Britax Child Safety

Official ID 26C006000 · Official record ↗

CPSC · Consumer Product · August 20, 2026

CCM Hockey U.S. Recalls FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories Due to Risk of Injury from Laceration or Impact Hazards

The recalled hockey visors and replacement visor accessories can crack upon impact, posing a risk of injury due to laceration or impact hazards.

Company / brand: CCM Hockey U.S

Official ID 26716 · Official notice ↗

CPSC · Consumer Product · August 20, 2026

Workbless Pressure Washers Recalled Due to Risk of Serious Injury or Death from Shock and Electrocution Hazards

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing serious risks of injury or death from shock and ele…

Company / brand: Guangzhou Ao Lian Ya Wang Luo Ke Ji You Xian Gong Si

Official ID 26715 · Official notice ↗

CPSC · Consumer Product · August 20, 2026

Koorlian Mattresses Recalled Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability; Sold on Amazon by Dream Bedding Technology

The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire.

Company / brand: Dreams Bedding Technology PTE

Official ID 26714 · Official notice ↗

CPSC · Consumer Product · August 20, 2026

JINHEZO Mini Waterproof LED Tea Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries; Imported by Mystic ZO

The LED Tea Lights violate the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can be accessed easily by children, …

Company / brand: Shenzhen Jinhe Trade Co

Official ID 26713 · Official notice ↗

CPSC · Consumer Product · August 20, 2026

Goal Zero Recalls YETI 3000X Power Stations Due to Serious Risk of Injury from Fire and Burn Hazards

The recalled power station's circuit board can overheat, posing a risk of serious injury from fire and burn hazards.

Company / brand: Goal Zero

Official ID 26712 · Official notice ↗

CPSC · Consumer Product · August 20, 2026

Modine Manufacturing Company Recalls Airedale Heating and Cooling Ventilation Fans Due to Fire Hazard

The ventilation fan motor in the heat pumps can short circuit if water gets on the circuit board, causing the units to overheat and posing a fire hazard.

Company / brand: Modine Manufacturing Company

Official ID 26711 · Official notice ↗

CPSC · Consumer Product · August 20, 2026

KTM North America Recalls Off-Road Motorcycles Due to Risk of Serious Injury or Death from Crash Hazard

The rear brake caliper can crack or break, reducing the brake system's effectiveness, posing a risk of serious injury or death due to crash hazard.

Company / brand: KTM North America

Official ID 26710 · Official notice ↗

NHTSA · Vehicle · August 19, 2026

E-One Incorporated Equipment recall (26V537000)

The inability to extend or retract the outriggers can delay emergency response, increasing the risk of injury.

Company / brand: E-One Incorporated

Official ID 26V537000 · Official record ↗

NHTSA · Vehicle equipment · August 19, 2026

Avride Automated Driving System recall (26E059000)

Unexpected vehicle movement may increase the risk of a crash.

Company / brand: Avride

Official ID 26E059000 · Official record ↗

FDA Not Yet Classified · Drug · August 19, 2026

Cefazolin in Dextrose recall — Baxter Healthcare Corporation

Presence of Particulate Matter

Company / brand: Baxter Healthcare

Official ID EVT-99463-1krekt6 · Official record ↗

FDA Not Yet Classified · Food · August 19, 2026

MARKON BLEND LETT/ROM 80/20 WITH SEP BAGGIES 4/5# Iceberg recall — Taylor Farms de Mexico S. de R.L. de C.V.

Potential Cyclospora contamination.

Company / brand: Taylor Farms de Mexico S. de R.L. de C.V

Official ID EVT-99453-wgl5uq · Official record ↗

FDA Class II · Medical device · August 19, 2026

Cardinal Health Presource Kits recall — Cardinal Health 200, LLC

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

Company / brand: Cardinal Health 200

Official ID Z-2949-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Cardinal Health Presource Kits recall — Cardinal Health 200, LLC

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

Company / brand: Cardinal Health 200

Official ID Z-2948-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Cardinal Health Presource Kits recall — Cardinal Health 200, LLC

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

Company / brand: Cardinal Health 200

Official ID Z-2947-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Cardinal Health Presource Kits recall — Cardinal Health 200, LLC

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

Company / brand: Cardinal Health 200

Official ID Z-2946-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Cardinal Health Presource Kits recall — Cardinal Health 200, LLC

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

Company / brand: Cardinal Health 200

Official ID Z-2945-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Cardinal Health Presource Kits recall — Cardinal Health 200, LLC

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

Company / brand: Cardinal Health 200

Official ID Z-2944-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Cardinal Health Presource Kits recall — Cardinal Health 200, LLC

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

Company / brand: Cardinal Health 200

Official ID Z-2943-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Cardinal Health Presource Kits recall — Cardinal Health 200, LLC

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

Company / brand: Cardinal Health 200

Official ID Z-2942-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code recall — BD SWITZERLAND SARL

Products may not have received adequate sterilization processing.

Company / brand: BD SWITZERLAND SARL

Official ID Z-2941-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

ERBECRYO 2 Cryosurgical Unit Model/Catalog Number recall — Erbe USA Inc

A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector resulting in CO2 leaking into the r…

Company / brand: Erbe USA

Official ID Z-2938-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

ProNephro AKI (NGAL) Reagent Kit (100 tests) recall — Bioporto Diagnostics A/S

The use of a non-validated rework process for assay reagents which could lead to missed diagnosis of renal disease, inappropriate treatment decisions, or inappropriate monitoring o…

Company / brand: Bioporto Diagnostics A/S

Official ID Z-2937-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

BIOFIRE Respiratory Panel 2 recall — BioFire Diagnostics, LLC

Due to increase in false negative results

Company / brand: BioFire Diagnostics

Official ID Z-2936-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Straumann Bone Level Tapered (BLT) Implant recall — Straumann USA LLC

Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the labeling would suggest…

Company / brand: Straumann USA

Official ID Z-2935-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Endo-Model recall — Waldemar Link GmbH & Co. KG (Mfg Site)

The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a prolonged or modified s…

Company / brand: Waldemar Link & Co. KG (Mfg Site)

Official ID Z-2934-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

OBP Medical recall — OBP Medical Corporation

There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the hea…

Company / brand: OBP Medical

Official ID Z-2933-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Philips Azurion recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Two software related issues: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment and 2) Potential loss…

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V

Official ID Z-2932-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Philips Azurion Rystem recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropria…

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V

Official ID Z-2931-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

GLIDESHEATH SLENDER A-KIT 6F 10CM recall — Terumo Medical Corporation

Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.

Company / brand: Terumo Medical

Official ID Z-2930-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

GM Helix Implant recall — Straumann USA LLC

There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect implant is installed, the i…

Company / brand: Straumann USA

Official ID Z-2929-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Allura Xper FD recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Firmware issue potentially leading to loss of geometry movements.

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V

Official ID Z-2928-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL recall — Remel Europe Ltd.

Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds.

Company / brand: Remel Europe

Official ID Z-2927-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Medline Micro-Kill Bleach Germicidal Bleach Wipes recall — Medline Industries, LP

Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life.…

Company / brand: Medline Industries

Official ID Z-2926-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Medline Micro-Kill Bleach Germicidal Bleach Wipes recall — Medline Industries, LP

Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life.…

Company / brand: Medline Industries

Official ID Z-2925-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Medline Micro-Kill Bleach Germicidal Bleach Wipes recall — Medline Industries, LP

Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life.…

Company / brand: Medline Industries

Official ID Z-2924-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Medline Micro-Kill Bleach Germicidal Bleach Wipes recall — Medline Industries, LP

Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life.…

Company / brand: Medline Industries

Official ID Z-2923-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX recall — Covidien, LP

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v…

Company / brand: Covidien

Official ID Z-2922-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623 recall — Covidien, LP

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v…

Company / brand: Covidien

Official ID Z-2921-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU recall — Covidien, LP

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v…

Company / brand: Covidien

Official ID Z-2920-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING BOX06614V4 BOX BY P recall — Covidien, LP

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v…

Company / brand: Covidien

Official ID Z-2919-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22 G recall — Covidien, LP

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v…

Company / brand: Covidien

Official ID Z-2918-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF recall — Galt Medical Corporation

Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits.

Company / brand: Galt Medical

Official ID Z-2917-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Brand Name recall — Spacelabs Healthcare, Inc.

Due to off-the-shelf display port component that has audio/video failures

Company / brand: Spacelabs Healthcare

Official ID Z-2916-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

GORE VIABIL Short Wire Biliary Endoprosthesis recall — W L Gore & Associates, Inc.

10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes (VSWVN1010).

Company / brand: W L Gore & Associates

Official ID Z-2915-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

GORE VIABIL Short Wire Biliary Endoprosthesis recall — W L Gore & Associates, Inc.

10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes (VSWVN1010).

Company / brand: W L Gore & Associates

Official ID Z-2914-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

navify Digital Pathology (on-prem) v2 recall — Ventana Medical Systems, Inc.

Due to complaints received for the Image Management System regarding image/metadata discrepancy with the Viewer window

Company / brand: Ventana Medical Systems

Official ID Z-2913-2026 · Official record ↗

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Government sources last checked September 7, 2026 at 6:00 AM UTC.