Latest recalls — page 14

Undeclared Soy. The firm received complaints of sausage in the burritos. Upon review the firm discovered the sausage contains soy which is not listed on the label.

Company / brand: M.G. Foods recalls

Official ID H-1192-2026 · Official record ↗

FDA Class II · Drug · August 12, 2026

Mirabegron Extended-Release Tablets recall — Zydus Pharmaceuticals (USA) Inc

CGMP: Due to Out of Specification (OOS) result for N-Nitroso Mirabegron impurity.

Company / brand: Zydus Pharmaceuticals (USA) recalls

Official ID D-0745-2026 · Official record ↗

FDA Class I · Drug · August 12, 2026

Cyclophosphamide for Injection recall — Sunny Pharmtech Inc.

Presence of Particulate Matter; identified as stainless steel

Company / brand: Sunny Pharmtech recalls

Official ID D-0744-2026 · Official record ↗

FDA Class I · Drug · August 12, 2026

Cyclophosphamide for Injection recall — Sunny Pharmtech Inc.

Presence of Particulate Matter; identified as stainless steel

Company / brand: Sunny Pharmtech recalls

Official ID D-0743-2026 · Official record ↗

FDA Class III · Drug · August 12, 2026

Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag recall — Central Admixture Pharmacy Services Inc

Incorrect Product Formulation

Company / brand: Central Admixture Pharmacy Services recalls

Official ID D-0740-2026 · Official record ↗

FDA Class II · Drug · August 12, 2026

Dicyclomine Hydrochloride Capsules recall — Aurobindo Pharma USA Inc

shortfill; reports of empty capsules.

Company / brand: Aurobindo Pharma USA recalls

Official ID D-0733-2026 · Official record ↗

NHTSA · Vehicle · August 10, 2026

Thomas Built Buses Saf-T-Liner C2 recall (26V523000)

During a crash, an incompatible fuel tank cage and fuel system may result in a fuel leak, increasing the risk of a fire.

Company / brand: Daimler Trucks North America recalls

Official ID 26V523000 · Official record ↗

NHTSA · Vehicle · August 10, 2026

Thomas Built Buses Saf-T-Liner C2 recall (26V522000)

During a crash, an incompatible fuel tank cage and fuel system may result in a fuel leak, increasing the risk of a fire.

Company / brand: Daimler Trucks North America recalls

Official ID 26V522000 · Official record ↗

NHTSA · Vehicle · August 10, 2026

Marion Pumper recall (26V521000)

A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Inoperative equipment can delay emergency response, increasing …

Company / brand: Marion Body Works recalls

Official ID 26V521000 · Official record ↗

NHTSA · Vehicle · August 10, 2026

Blue Bird Vision Transit Bus recall (26V520000)

An electrical short can cause a disruption to safety functions such as a loss of rear lighting or instrument panel warning lights, increasing the risk of a crash.

Company / brand: Blue Bird Body Company recalls

Official ID 26V520000 · Official record ↗

NHTSA · Vehicle · August 10, 2026

Blue Bird Body Company Electrical System recall (26V519000)

An electrical short can cause a disruption to safety functions such as a loss of rear lighting or instrument panel warning lights, increasing the risk of a crash.

Company / brand: Blue Bird Body Company recalls

Official ID 26V519000 · Official record ↗

NHTSA · Vehicle · August 6, 2026

Jayco Electrical System recall (26V518000)

Activation of the jacks during transit increases the risk of a crash.

Company / brand: Jayco recalls

Official ID 26V518000 · Official record ↗

NHTSA · Vehicle · August 6, 2026

Isuzu NPR HD recall (26V517000)

A liftgate that falls unexpectedly increases the risk of injury.

Company / brand: US Truck Body CO recalls

Official ID 26V517000 · Official record ↗

NHTSA · Vehicle · August 6, 2026

International Motors Visibility recall (26V516000)

Inoperative windshield wipers can reduce the driver's visibility, increasing the risk of a crash.

Company / brand: International Motors recalls

Official ID 26V516000 · Official record ↗

NHTSA · Vehicle · August 6, 2026

Mack Trucks Exterior Lighting recall (26V515000)

Marker lights that fail to illuminate can reduce visibility, increasing the risk of a crash.

Company / brand: Mack Trucks recalls

Official ID 26V515000 · Official record ↗

NHTSA · Vehicle · August 6, 2026

Toyota Motor Engineering & Manufacturing Suspension recall (26V514000)

An oil reservoir that detaches can create a road hazard, increasing the risk of a crash.

Company / brand: Toyota Motor Engineering & Manufacturing recalls

Official ID 26V514000 · Official record ↗

NHTSA · Vehicle · August 6, 2026

Volvo Trucks North America Exterior Lighting recall (26V513000)

Marker lights that fail to illuminate can reduce visibility, increasing the risk of a crash.

Company / brand: Volvo Trucks North America recalls

Official ID 26V513000 · Official record ↗

NHTSA · Vehicle · August 6, 2026

Toyota BZ Woodland recall (26V512000)

Driving with a disabled electronic stability control system or continuously illuminated brake lights can increase the risk of a crash.

Company / brand: Toyota Motor Engineering & Manufacturing recalls

Official ID 26V512000 · Official record ↗

NHTSA · Vehicle · August 6, 2026

Toyota Camry Hybrid recall (26V511000)

An instrument cluster that fails to display critical safety information increases the risk of a crash or injury.

Company / brand: Toyota Motor Engineering & Manufacturing recalls

Official ID 26V511000 · Official record ↗

NHTSA · Vehicle · August 6, 2026

Chrysler Seat Belts recall (26V510000)

A seat belt that does not retract may fail to restrain properly an occupant as intended, increasing the risk of injury.

Company / brand: Chrysler recalls

Official ID 26V510000 · Official record ↗

NHTSA · Vehicle · August 6, 2026

Mack Terrapro (TE) recall (26V509000)

A loose steering gearbox can result in a loss of steering, increasing the risk of a crash.

Company / brand: Mack Trucks recalls

Official ID 26V509000 · Official record ↗

NHTSA · Vehicle · August 6, 2026

Rivian Automotive Exterior Lighting recall (26V508000)

Turn signals that do not function properly increase the risk of a crash.

Company / brand: Rivian Automotive recalls

Official ID 26V508000 · Official record ↗

NHTSA · Vehicle equipment · August 6, 2026

Chrysler recall (26E053000)

A seat belt that does not retract properly may fail to restrain an occupant as intended, increasing the risk of injury.

Company / brand: Chrysler recalls

Official ID 26E053000 · Official record ↗

NHTSA · Child car seat · August 6, 2026

Evenflo Company recall (26C005000)

A child seat that is not reclined as intended increases the risk of injury in a crash.

Company / brand: Evenflo Company recalls

Official ID 26C005000 · Official record ↗

CPSC · Consumer Product · August 6, 2026

Head Watersports Recalls Apeks Second Stage Scuba Regulators Recalled Due to Risk of Serious Injury or Death from Drowning Hazard

The recalled second stage regulators can restrict air flow to the user at depths exceeding 45 meters (approximately 147 feet), posing risk of serious injury or death from a drownin…

Company / brand: HEAD USA recalls

Official ID 26677 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

Fitueyes Recalls Laziza 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: Fitueyes recalls

Official ID 26676 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

Wichard Groupe North America Recalls Courant Spliced Kalimba Climbing Ropes Due to Risk of Serious Injury or Death from Fall Hazard

The spliced termination ends on the recalled ropes can fail unexpectedly, posing a risk of serious injury or death from fall hazard.

Company / brand: Courant recalls

Official ID 26675 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

Vanderhall North America Recalls Brawley GTS Electric Recreational Off Highway Vehicles (ROVs) Due to Risk of Serious Injury or Death from Crash Hazard

The recalled recreational off highway vehicle can maintain speed or accelerate when the accelerator pedal is released, posing a risk of serious injury or death from a crash hazard.

Company / brand: Vanderhall North America recalls

Official ID 26674 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

KC Imports and Exports Recalls Mini Laser Pointer Keychains Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries

The Mini Laser Pointer Keychains violate the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can be accessed easily…

Company / brand: KC IMPORTS AND EXPORTS recalls

Official ID 26673 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

Syera Projecting Finger Light Toys Recalled Due to Risk of Serious Injury from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on TEMU by Senyu

The recalled LED finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children. If button cell or …

Company / brand: Senyu Era International Co recalls

Official ID 26672 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

Little Rawr Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Okabesini-us

The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of children's …

Company / brand: Shenzhen Okabesini Technology Co recalls

Official ID 26671 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

A2batt Recalls EEMB Lithium Coin Battery Chargers Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries

The recalled battery chargers violate the mandatory standard for consumer products containing button cell or coin batteries, because the charger has lithium coin batteries that can…

Company / brand: EEMB USA recalls

Official ID 26670 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

Play Yard and Crib Mattresses Recalled Due to Risk of Serious Injury or Death from Entrapment and Fire Hazards; Violate Mandatory Standards for Mattresses; Sold on Amazon by Voomf

The recalled mattresses violate the mandatory safety standard for crib mattresses because the mattresses may not adequately fit certain play yards, posing a deadly entrapment hazar…

Company / brand: Shanghaiyuejiuyaoguojimaoyiyouxiangongsi (Shanghai Yuejiuyao International Trade Co recalls

Official ID 26669 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

Liuqibax Adult 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 Luqiba

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: Changsha 678 Trading Co recalls

Official ID 26668 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

Magnetic Fidget Sliders Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by PIXLABBY

The magnetic fidget sliders violate the mandatory standard for toys because they can liberate loose high-powered magnets posing an ingestion hazard to children. When high-powered m…

Company / brand: Huoshan County Haozhou E-commerce Co recalls

Official ID 26667 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

Wnttmt Baby Walkers Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violate Mandatory Standard for Infant Walkers; Sold on Amazon by WURUI.BABY

The recalled infant 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 deadl…

Company / brand: Changsha Yuelu District Ruiwu E-Commerce Co recalls

Official ID 26665 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

Magnetic Fidget Sliders Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys: Sold on Amazon by BUSOHA

The magnetic fidget sliders violate the mandatory standard for toys because they can liberate loose magnets posing an ingestion hazard to children. When high-powered magnets are sw…

Company / brand: Shenzhen Yuejia Mei Maoyi Youxian Gongsi (Shenzhen Yuejia Mei Trading Co recalls

Official ID 26664 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

Winston Porter and Seeday 3-Drawer, 4-Drawer, and 5-Drawer Dressers Recalled 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: Linyi Lingmoxuan Technology Co recalls

Official ID 26663 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

OKK Trading Recalls Easter LED Headbands Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys

The recalled headbands violate the mandatory safety standard for toys with button cell and coin batteries because the lithium coin batteries can be accessed easily by children, pos…

Company / brand: OKK Trading recalls

Official ID 26662 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

Louisville Ladder Recalls Over One Million Attic Stairway Ladders Due to Risk of Serious Injury or Death from Fall Hazard

The bolts on the attic stairway ladders can break while in use, posing a risk of serious injury or death from fall hazard.

Company / brand: Louisville Ladder recalls

Official ID 26661 · Official notice ↗

CPSC · Consumer Product · August 6, 2026

DR Power Equipment Recalls Lawn Mowers Due to Risk of Serious Injury or Death from Laceration Hazard; Violate Mandatory Standard for Lawn Mowers

The recalled mowers violate the mandatory safety standard for walk-behind power lawn mowers because the blades can operate without the blade control system engaged or continue to o…

Company / brand: Generac Power Systems recalls

Official ID 26648 · Official notice ↗

NHTSA · Vehicle · August 5, 2026

Tesla Exterior Lighting recall (26V507000)

Headlight low beams that are too bright can reduce visibility for oncoming drivers, increasing the risk of a crash.

Company / brand: Tesla recalls

Official ID 26V507000 · Official record ↗

FDA Not Yet Classified · Drug · August 5, 2026

Dabigatran Etexilate Capsules recall — Ascend Laboratories, LLC

Failed impurity/degradation specification:12M Long-term Stability conditions (25 ¿2 ¿C/60 ¿5%RH), an OOS result observed in Related substance test analysis w.r.t Impurity II, Impur…

Company / brand: Ascend Laboratories recalls

Official ID EVT-99421-191x326 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 150mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Company / brand: Stryker recalls

Official ID Z-2833-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 120mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Company / brand: Stryker recalls

Official ID Z-2832-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 90mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Company / brand: Stryker recalls

Official ID Z-2831-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 60mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Company / brand: Stryker recalls

Official ID Z-2830-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 50mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Company / brand: Stryker recalls

Official ID Z-2829-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 40mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Company / brand: Stryker recalls

Official ID Z-2828-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 30mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Company / brand: Stryker recalls

Official ID Z-2827-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Brand Name recall — Instrumentation Laboratory

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Company / brand: Instrumentation Laboratory recalls

Official ID Z-2826-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Brand Name recall — Instrumentation Laboratory

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Company / brand: Instrumentation Laboratory recalls

Official ID Z-2825-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Brand Name recall — Instrumentation Laboratory

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Company / brand: Instrumentation Laboratory recalls

Official ID Z-2824-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Brand Name recall — Instrumentation Laboratory

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Company / brand: Instrumentation Laboratory recalls

Official ID Z-2823-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Brand Name recall — Instrumentation Laboratory

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Company / brand: Instrumentation Laboratory recalls

Official ID Z-2822-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

GEM Premier 5000 with IQM2 Model/Catalog Number recall — Instrumentation Laboratory

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Company / brand: Instrumentation Laboratory recalls

Official ID Z-2821-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

OsteoBallast recall — IsoTis OrthoBiologics, Inc.

Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were filled with approx. 4.5 cc…

Company / brand: IsoTis OrthoBiologics recalls

Official ID Z-2820-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2819-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2818-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2817-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2816-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2815-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2814-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2813-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2812-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

EOPA 3D Arterial Cannula 22FR recall — Medtronic Perfusion Systems

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…

Company / brand: Medtronic Perfusion Systems recalls

Official ID Z-2811-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

EOPA 3D Arterial Cannula DIL TIP 22FR recall — Medtronic Perfusion Systems

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…

Company / brand: Medtronic Perfusion Systems recalls

Official ID Z-2810-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR recall — Medtronic Perfusion Systems

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…

Company / brand: Medtronic Perfusion Systems recalls

Official ID Z-2809-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR recall — Medtronic Perfusion Systems

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…

Company / brand: Medtronic Perfusion Systems recalls

Official ID Z-2808-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR recall — Medtronic Perfusion Systems

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…

Company / brand: Medtronic Perfusion Systems recalls

Official ID Z-2807-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR recall — Medtronic Perfusion Systems

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…

Company / brand: Medtronic Perfusion Systems recalls

Official ID Z-2806-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

M5 Corpus Power Wheelchair REF recall — Permobil Inc

This recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic. This issue may allow the chair to drive under restricted conditions, a…

Company / brand: Permobil recalls

Official ID Z-2805-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm recall — Argon Medical Devices, Inc

Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking a…

Company / brand: Argon Medical Devices recalls

Official ID Z-2804-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

L-Cath PICC S/L Peripherally Inserted Central Catheter recall — Argon Medical Devices, Inc

Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking a…

Company / brand: Argon Medical Devices recalls

Official ID Z-2803-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2802-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2801-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2800-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2799-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF recall — Permobil Inc

This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the use…

Company / brand: Permobil recalls

Official ID Z-2795-2026 · Official record ↗

FDA Class I · Medical device · August 5, 2026

Pack Angiography NCMC 3/Cs BANNER recall — Medical Action Industries, Inc. 306

Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood…

Company / brand: Medical Action Industries recalls

Official ID Z-2792-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Power Over Fiber Base Module recall — Terex Utilities

Device not certified - no laser product report was filed with CDRH prior to distribution. Product label incorrectly states device is "Class IV", although Class 1 is appropriate for…

Company / brand: Terex Utilities recalls

Official ID Z-2745-2026 · Official record ↗

FDA Class I · Medical device · August 5, 2026

Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous recall — ResMed Ltd.

Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of ventilation therapy.

Company / brand: ResMed recalls

Official ID Z-2735-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro CT5000 Ingenuity Premium Ingenuity recall — PHILIPS MEDICAL SYSTEMS

The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result i…

Company / brand: PHILIPS MEDICAL SYSTEMS recalls

Official ID Z-2652-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

IQon Spectral CT IQon Spectral CT Upgrades recall — PHILIPS MEDICAL SYSTEMS

The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result i…

Company / brand: PHILIPS MEDICAL SYSTEMS recalls

Official ID Z-2651-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 B recall — PHILIPS MEDICAL SYSTEMS

The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result i…

Company / brand: PHILIPS MEDICAL SYSTEMS recalls

Official ID Z-2650-2026 · Official record ↗

FDA Class II · Food · August 5, 2026