Fresh Recalls

Latest recalls — page 17

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

3,525 recalls in our current data. Showing 1,601–1,700, newest first.

FDA Class I · Medical device · July 22, 2026

ABIOMED Impella CP Set recall — Abiomed, Inc.

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…

Company / brand: Abiomed recalls

Official ID Z-2689-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

ABIOMED Impella 5 recall — Abiomed, Inc.

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…

Company / brand: Abiomed recalls

Official ID Z-2688-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

ABIOMED Impella 5 recall — Abiomed, Inc.

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…

Company / brand: Abiomed recalls

Official ID Z-2687-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

ABIOMED Impella CP Introducer Kit 14 Fr recall — Abiomed, Inc.

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…

Company / brand: Abiomed recalls

Official ID Z-2686-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

ABIOMED Impella CP Introducer Kit 14 Fr recall — Abiomed, Inc.

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…

Company / brand: Abiomed recalls

Official ID Z-2685-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

ABIOMED Introducer Kit 23 Fr recall — Abiomed, Inc.

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…

Company / brand: Abiomed recalls

Official ID Z-2684-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

ABIOMED Impella CP Introducer Kit 14 Fr recall — Abiomed, Inc.

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…

Company / brand: Abiomed recalls

Official ID Z-2683-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

ABIOMED Impella CP Set recall — Abiomed, Inc.

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…

Company / brand: Abiomed recalls

Official ID Z-2682-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

ABIOMED Impella RP Flex with SmartAssist Set recall — Abiomed, Inc.

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…

Company / brand: Abiomed recalls

Official ID Z-2681-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

Abiomed REF recall — Oscor Inc.

Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub …

Company / brand: Oscor recalls

Official ID Z-2680-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

Abiomed REF recall — Oscor Inc.

Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub …

Company / brand: Oscor recalls

Official ID Z-2679-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

Abiomed REF recall — Oscor Inc.

Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub …

Company / brand: Oscor recalls

Official ID Z-2678-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Organic Whole Blueberries recall — Frutas y Hortalizas del Sur S.A.

Potential E. coli O145:H28 Contamination

Company / brand: Frutas y Hortalizas del Sur recalls

Official ID H-1181-2026 · Official record ↗

FDA Class II · Food · July 22, 2026

Ruby recall — GELLERT GLOBAL GROUP

Foreign material (Glass) was found in the product.

Company / brand: GELLERT GLOBAL GROUP recalls

Official ID H-1176-2026 · Official record ↗

FDA Class II · Food · July 22, 2026

OLA-OLA POUNDED GROUNDNUTS (INTWILO) NET WT recall — Fayus Inc.

Undeclared peanuts

Company / brand: Fayus recalls

Official ID H-1175-2026 · Official record ↗

FDA Class II · Food · July 22, 2026

Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT recall — AMY'S KITCHEN INC.

Potential for spoilage.

Company / brand: AMY'S KITCHEN recalls

Official ID H-1174-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1173-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1172-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1171-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1170-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1169-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1168-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1167-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1166-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1165-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1164-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1163-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1162-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1161-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1160-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1159-2026 · Official record ↗

FDA Class I · Food · July 22, 2026

Ice Pop recall — D'Dioses Fruit Pops, Inc.

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Company / brand: D'Dioses Fruit Pops recalls

Official ID H-1158-2026 · Official record ↗

FDA Class II · Food · July 22, 2026

WY Duck Sauce recall — W.Y. Industries, Inc.

Product may contain metal fragments.

Company / brand: W.Y. Industries recalls

Official ID H-1157-2026 · Official record ↗

FDA Class II · Food · July 22, 2026

Winfield's CWB Chocolate Bar recall — Chocolate Bar Holdings LLC

Undeclared milk allergen.

Company / brand: Chocolate Bar Holdings recalls

Official ID H-1156-2026 · Official record ↗

FDA Class II · Food · July 22, 2026

Pillsbury Bread Rolls recall — General Mills James Ford Bell Technical Center

Potential foreign material (glass)

Company / brand: General Mills James Ford Bell Technical Center recalls

Official ID H-1155-2026 · Official record ↗

FDA Class II · Food · July 22, 2026

Pillsbury Bread Rolls recall — General Mills James Ford Bell Technical Center

Potential foreign material (glass)

Company / brand: General Mills James Ford Bell Technical Center recalls

Official ID H-1154-2026 · Official record ↗

FDA Class II · Food · July 22, 2026

functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY recall — Nutricia North America

Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A…

Company / brand: Nutricia North America recalls

Official ID H-1153-2026 · Official record ↗

FDA Class II · Food · July 22, 2026

functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BE recall — Nutricia North America

Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A…

Company / brand: Nutricia North America recalls

Official ID H-1152-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

BD ChloraPrep Clear recall — CareFusion 213, LLC

Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator

Company / brand: CareFusion 213 recalls

Official ID D-0690-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

CLEVIPREX (clevidipine injectable emulsion) 50 mg/100 mL (0 recall — Chiesi USA, Inc.

Lack of Assurance of Sterility

Company / brand: Chiesi USA recalls

Official ID D-0689-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

CAREone recall — Bell Pharmaceuticals, Inc

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Company / brand: Bell Pharmaceuticals recalls

Official ID D-0688-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

meijer recall — Bell Pharmaceuticals, Inc

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Company / brand: Bell Pharmaceuticals recalls

Official ID D-0687-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

Foster & Thrive recall — Bell Pharmaceuticals, Inc

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Company / brand: Bell Pharmaceuticals recalls

Official ID D-0686-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

LEADER recall — Bell Pharmaceuticals, Inc

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Company / brand: Bell Pharmaceuticals recalls

Official ID D-0685-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

GOOD NEIGHBOR PHARMACY recall — Bell Pharmaceuticals, Inc

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Company / brand: Bell Pharmaceuticals recalls

Official ID D-0684-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

FAMILY Wellness recall — Bell Pharmaceuticals, Inc

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Company / brand: Bell Pharmaceuticals recalls

Official ID D-0683-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

AUDIOLOGIST'S CHOICE recall — Bell Pharmaceuticals, Inc

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Company / brand: Bell Pharmaceuticals recalls

Official ID D-0682-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

TopCare Health recall — Bell Pharmaceuticals, Inc

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Company / brand: Bell Pharmaceuticals recalls

Official ID D-0681-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

QC Quality Choice recall — Bell Pharmaceuticals, Inc

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Company / brand: Bell Pharmaceuticals recalls

Official ID D-0680-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

Clinere recall — Bell Pharmaceuticals, Inc

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Company / brand: Bell Pharmaceuticals recalls

Official ID D-0679-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

CVS Health recall — Bell Pharmaceuticals, Inc

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Company / brand: Bell Pharmaceuticals recalls

Official ID D-0678-2026 · Official record ↗

FDA Class II · Drug · July 22, 2026

Nystatin Cream USP recall — Padagis US LLC

Subpotent Drug: Low out of specification assay results performed during long-term stability testing.

Company / brand: Padagis US recalls

Official ID D-0677-2026 · Official record ↗

NHTSA · Vehicle · July 21, 2026

Ford Motor Company Seats recall (26V470000)

Unexpected movement of the driver’s seat back may trap a second-row occupant, increasing the risk of injury.

Company / brand: Ford Motor Company recalls

Official ID 26V470000 · Official record ↗

NHTSA · Vehicle · July 21, 2026

Ember Recreational Vehicles Equipment recall (26V469000)

An incorrect VIN on the label can make it difficult for owners to recognize that their vehicle is involved in a safety recall, increasing the risk of crash or injury.

Company / brand: Ember Recreational Vehicles recalls

Official ID 26V469000 · Official record ↗

NHTSA · Vehicle · July 20, 2026

Ford Bronco recall (26V468000)

A short circuit in the engine compartment can create heat or spark, increasing the risk of a fire.

Company / brand: Ford Motor Company recalls

Official ID 26V468000 · Official record ↗

NHTSA · Vehicle · July 20, 2026

Blue Bird Vision Transit Bus recall (26V467000)

A brake fluid leak in the presence of an ignition source such as hot engine or exhaust components can increase the risk of a fire. Additionally, a brake fluid leak can extend the d…

Company / brand: Blue Bird Body Company recalls

Official ID 26V467000 · Official record ↗

NHTSA · Vehicle · July 20, 2026

Blue Bird Vision School Bus recall (26V466000)

A brake fluid leak in the presence of an ignition source such as hot engine or exhaust components can increase the risk of a fire. Additionally, a brake fluid leak can extend the d…

Company / brand: Blue Bird Body Company recalls

Official ID 26V466000 · Official record ↗

NHTSA · Vehicle · July 17, 2026

Great Dane Champion recall (26V465000)

A rear impact guard that is not properly installed can increase the risk of injury during a crash.

Company / brand: Great Dane Trailers recalls

Official ID 26V465000 · Official record ↗

NHTSA · Vehicle · July 17, 2026

Foretravel Realm recall (26V464000)

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

Company / brand: Foretravel recalls

Official ID 26V464000 · Official record ↗

NHTSA · Vehicle · July 17, 2026

Altec At Series recall (26V463000)

A fastener that has not been heat treated could fail, resulting in separation of the pedestal and turntable, increasing the risk of injury.

Company / brand: Altec Industries recalls

Official ID 26V463000 · Official record ↗

NHTSA · Vehicle · July 17, 2026

Turtle Top Terra Ford Transit recall (26V462000)

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

Company / brand: Turtle Top recalls

Official ID 26V462000 · Official record ↗

NHTSA · Child car seat · July 17, 2026

Evenflo Company recall (26C004000)

A headrest that shifts unexpectedly may increase the risk of injury in a crash.

Company / brand: Evenflo Company recalls

Official ID 26C004000 · Official record ↗

NHTSA · Vehicle · July 16, 2026

IC Bus Cecb recall (26V461000)

The body panels may separate during a crash, reducing structural integrity and increasing the risk of injury.

Company / brand: International Motors recalls

Official ID 26V461000 · Official record ↗

NHTSA · Vehicle · July 16, 2026

International Motors Structure recall (26V460000)

The body panels may separate during a crash, reducing structural integrity and increasing the risk of injury.

Company / brand: International Motors recalls

Official ID 26V460000 · Official record ↗

NHTSA · Vehicle · July 16, 2026

International Motors Electrical System recall (26V459000)

A short circuit increases the risk of a fire.

Company / brand: International Motors recalls

Official ID 26V459000 · Official record ↗

NHTSA · Vehicle · July 16, 2026

Land Rover Discovery recall (26V458000)

A rearview camera image that does not display can decrease the driver's visibility, increasing the risk of a crash.

Company / brand: Jaguar Land Rover North America recalls

Official ID 26V458000 · Official record ↗

NHTSA · Vehicle · July 16, 2026

Altec AP Series recall (26V457000)

An overheated wire can ignite flammable material in the cargo area, increasing the risk of fire.

Company / brand: Altec Industries recalls

Official ID 26V457000 · Official record ↗

NHTSA · Vehicle · July 16, 2026

Chrysler Wheels recall (26V456000)

Loss of vehicle control increases the risk of a crash.

Company / brand: Chrysler recalls

Official ID 26V456000 · Official record ↗

CPSC · Consumer Product · July 16, 2026

MNIENT 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

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: Zhuzhoushizuisuanshangmaoyouxiangongsi recalls

Official ID 26630 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

Target Recalls Cat & Jack Children's Sandals Due to Risk of Serious Injury or Death from Choking Hazard

The sandals' decorative pearls can fall off, posing a risk of serious injury or death from a choking hazard.

Company / brand: Target recalls

Official ID 26629 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

SDADI Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Yiwushi Bihe Trading

The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of serious injury and d…

Company / brand: Yiwushi Bihe Trading Co recalls

Official ID 26628 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

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

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: Dongguan Shinneng Huizheng Network Technology Co recalls

Official ID 26627 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

Jobon Torch Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violate Mandatory Standard for Multipurpose Lighters

The lighters violate the mandatory safety standard for multipurpose lighters because they do not have the required child-resistant mechanisms posing a risk of serious injury or dea…

Company / brand: Madewell recalls

Official ID 26626 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

Madewell Recalls Women's Sweaters Due to Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Clothing Textiles

The recalled sweaters violate the mandatory standard for clothing textiles, posing a risk of serious burn injuries or death.

Company / brand: J. Crew Group recalls

Official ID 26625 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

Huish Outdoors Recalls Hollis Diving Regulators Due to Risk of Serious Injury or Death from Drowning

The regulator inlet tube can crack and break, posing a risk of serious injury or death from drowning.

Company / brand: Huish Outdoors recalls

Official ID 26624 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

Warren James Recalls the Copper Cup Found in Flashgitz Relic Lunch Boxes Due to Risk of Serious Injury or Death from Lead Poisoning

The cup in the lunch boxes contains high lead concentration levels for drinking vessels, posing a lead poisoning hazard. Lead is toxic if ingested by adults or children and can cau…

Company / brand: Warren James recalls

Official ID 26623 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

Wade Logan Annyka 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Imported by Ningbo Jiangdong Peter International Trading

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: Wuxi Leclaire Home Products Co recalls

Official ID 26622 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

Currey & Company Recalls Nottaway Chandeliers Due to Risk of Serious Injury or Death from Electrocution Hazard

The recalled chandeliers lack proper electrical grounding, posing a risk of serious injury or death from electrocution hazard.

Company / brand: Currey & Company recalls

Official ID 26621 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

TOMY Recalls Boon PIVOT Collapsible Toddler Tower Kitchen Step Stools Due to Risk of Serious Injury and Death from Tip-Over and Fall Hazards

The recalled toddler towers can tip over while in use, posing a risk of serious injury and death, due to tip over and fall hazards.

Company / brand: TOMY International recalls

Official ID 26620 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

Liizousuda Paint Thinner Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging; Sold on Amazon.com by Shenzhen Gudebo Technology

The paint thinner contains low-viscosity petroleum distillates, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The bottles are not …

Company / brand: Shenzhen Gudebo Technology Co recalls

Official ID 26619 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

Panasonic Recalls Electric Toaster Ovens Due to Shock and Fire Hazards

The power cord insulation can be insufficient due to a protective fiberglass sleeve not covering it adequately, posing a risk of shock and/or fire hazard.

Company / brand: Panasonic Manufacturing (Xiamen) Co recalls

Official ID 26618 · Official notice ↗

CPSC · Consumer Product · July 16, 2026

Oitnlaughter Projecting Finger Light Toys Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Delightmi

The recalled 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 coin…

Company / brand: Shenzhen Dami Trading Co recalls

Official ID 26617 · Official notice ↗

NHTSA · Vehicle · July 15, 2026

Nissan North America Equipment recall (26V455000)

An overloaded vehicle can increase the risk of a crash.

Company / brand: Nissan North America recalls

Official ID 26V455000 · Official record ↗

NHTSA · Vehicle · July 15, 2026

E-One Incorporated Power Train recall (26V454000)

Loss of power to the rear wheels can prevent the vehicle from moving, increasing the risk of a crash.

Company / brand: E-One Incorporated recalls

Official ID 26V454000 · Official record ↗

NHTSA · Vehicle · July 15, 2026

Orange EV Structure recall (26V453000)

A detached rail can cause a loss of control, increasing the risk of injury.

Company / brand: Orange EV recalls

Official ID 26V453000 · Official record ↗

FDA Class II · Medical device · July 15, 2026

Brand Name recall — CMR SURGICAL LIMITED

Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk.

Company / brand: CMR SURGICAL recalls

Official ID Z-2717-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

TMINI Femur Tracking Array REF 109003 UDI-DI code recall — Think Surgical, Inc.

Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.

Company / brand: Think Surgical recalls

Official ID Z-2716-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

VITEK 2 AST-N447 TEST KIT Product reference 424620 recall — Biomerieux Inc

Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.

Company / brand: Biomerieux recalls

Official ID Z-2715-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

OmniTract Surgical Retractor System recall — Integra LifeSciences Corp. (NeuroSciences)

The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110 …

Company / brand: Integra LifeSciences (NeuroSciences) recalls

Official ID Z-2714-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

GSP Neonatal GALT Kit recall — WALLAC OY

Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient results.

Company / brand: WALLAC OY recalls

Official ID Z-2713-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

Brand Name recall — Elekta, Inc.

Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.

Company / brand: Elekta recalls

Official ID Z-2712-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

Brand Name recall — Elekta, Inc.

Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.

Company / brand: Elekta recalls

Official ID Z-2711-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

Brand Name recall — Elekta, Inc.

Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.

Company / brand: Elekta recalls

Official ID Z-2710-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

Atellica CH Enzymatic Hemoglobin A1c (A1c_E) recall — Siemens Healthcare Diagnostics, Inc.

The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely elevated HbA1c patien…

Company / brand: Siemens Healthcare Diagnostics recalls

Official ID Z-2703-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

5008X Blood Tubing Set recall — Fresenius Medical Care Holdings, Inc.

Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X CAREsystem.

Company / brand: Fresenius Medical Care Holdings recalls

Official ID Z-2702-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

Brand Name recall — Encore Medical, LP

Due to packaging discrepancy with incorrect product size mixed up.

Company / brand: Encore Medical recalls

Official ID Z-2701-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

Brand Name recall — Encore Medical, LP

Due to packaging discrepancy with incorrect product size mixed up.

Company / brand: Encore Medical recalls

Official ID Z-2700-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

KL Owen Custom Orthodontic Solution recall — Klowen Braces

A product error defect may cause incorrect bracket placement.

Company / brand: Klowen Braces recalls

Official ID Z-2699-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

MiniMed 780G Insulin Pump recall — Medtronic MiniMed, Inc.

A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error me…

Company / brand: Medtronic MiniMed recalls

Official ID Z-2698-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

Medline Convenience Kits recall — Medline Industries, LP

Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm ge…

Company / brand: Medline Industries recalls

Official ID Z-2697-2026 · Official record ↗

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Government sources last checked October 22, 2026 at 12:00 PM UTC.