États-Unis Recalls

Rappels de sécurité de la FDA, CPSC, NHTSA et de l’USDA FSIS.

Showing 24 of 17,563 results
Vehicle RecallUSNHTSA

General Motors, LLC - Improperly Secured Module May Damage High Voltage Battery

General Motors, LLC
NHTSAELECTRICAL SYSTEM

General Motors, LLC - Improperly Secured Module May Damage High Voltage Battery

A loose component may move and damage the high voltage battery, increasing the risk of a fire.

Jul 30, 2026General Motors, LLC
Vehicle RecallUSNHTSA

General Motors, LLC - Steel Wheels May Crack

General Motors, LLC
NHTSATIRES

General Motors, LLC - Steel Wheels May Crack

A cracked wheel may lead to disc separation and a loss of control, increasing the risk of a crash.

Jul 30, 2026General Motors, LLC
Safety AlertUSCPSC

Recall of Cpzzkq Baby Loungers Expanded Due to Risk Serious Injury or Death from Suffocation Hazard; Violate Mandatory Standard for Infant Support Cushions; Sold on Amazon by CetoPMax

Unknown Firm
Recall of Cpzzkq Baby Loungers Expanded Due to Risk Serious Injury or Death from Suffocation Hazard; Violate Mandatory Standard for Infant Support Cushions; Sold on Amazon by CetoPMax
CPSCGeneral Alert

Recall of Cpzzkq Baby Loungers Expanded Due to Risk Serious Injury or Death from Suffocation Hazard; Violate Mandatory Standard for Infant Support Cushions; Sold on Amazon by CetoPMax

The recalled baby loungers violate the mandatory safety standard for?infant support cushions?because the padding can obstruct an infant's breathing, posing a serious risk of injury or deadly suffocation hazard.

Jul 30, 2026
Safety AlertUSCPSC

Trsmima Zipline Kits and Zipline Spring Brakes Recalled Due to Fall and Collision Hazards; Manufactured by Trsmima

HuNanBoLuoDianZiShangWuYouXianGongSi D/B/A Trsmima or Hunan Pineapple Electronic Commerce Co., Ltd., of China
Trsmima Zipline Kits and Zipline Spring Brakes Recalled Due to Fall and Collision Hazards; Manufactured by Trsmima
CPSCGeneral Alert

Trsmima Zipline Kits and Zipline Spring Brakes Recalled Due to Fall and Collision Hazards; Manufactured by Trsmima

The zipline kit's steel cable, turnbuckle and seat can detach or break during use, posing a fall hazard. The zipline spring brakes are not stiff enough to safely slow a rider down and the kit design does not include an emergency brake, posing collision and fall hazards.

Jul 30, 2026HuNanBoLuoDianZiShangWuYouXianGongSi D/B/A Trsmima or Hunan Pineapple Electronic Commerce Co., Ltd., of China
Safety AlertUSCPSC

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; Sold on Amazon by KAIFAM

Unknown Firm
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; Sold on Amazon by KAIFAM
CPSCGeneral Alert

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; Sold on Amazon by KAIFAM

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. The dressers violate the mandatory safety standards as required by the STURDY Act.

Jul 30, 2026
Food & BeverageUSUSDA FSIS

FSIS Issues Public Health Alert for Chicken Salad Product that May Be Contaminated with Listeria

Mary's Harvest Fresh Foods, Inc.
USDA FSISPublic Health A...

FSIS Issues Public Health Alert for Chicken Salad Product that May Be Contaminated with Listeria

Product Contamination

Jul 30, 2026Mary's Harvest Fresh Foods, Inc.
Vehicle RecallUSNHTSA

Honda (American Honda Motor Co.) - Handlebar Lock Screw May Detach and Interfere with Steering

Honda (American Honda Motor Co.)
NHTSASTEERING

Honda (American Honda Motor Co.) - Handlebar Lock Screw May Detach and Interfere with Steering

A detached screw may lodge between the frame and stem, interfering with steering and increasing the risk of a crash or injury.

Jul 30, 2026Honda (American Honda Motor Co.)
Safety AlertUSCPSC

Woodure Toddler Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Shenzhen Muqiqu Creative Development

Unknown Firm
Woodure Toddler Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Shenzhen Muqiqu Creative Development
CPSCGeneral Alert

Woodure Toddler Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Shenzhen Muqiqu Creative Development

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 death due to tip over, fall and entrapment hazards.

Jul 30, 2026
Vehicle RecallUSNHTSA

Winnebago Industries, Inc. - Park Outside: Generator May Turn On Without Operator Action

Winnebago Industries, Inc.
NHTSAELECTRICAL SYSTEM

Winnebago Industries, Inc. - Park Outside: Generator May Turn On Without Operator Action

People in an enclosed space, such as a garage, with a running generator may be at an increased risk of injury or death from carbon monoxide poisoning.

Jul 30, 2026Winnebago Industries, Inc.
Safety AlertUSCPSC

Heated Sherpa Throws and Blankets Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Sold on Amazon by OCTROT

Unknown Firm
Heated Sherpa Throws and Blankets Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Sold on Amazon by OCTROT
CPSCGeneral Alert

Heated Sherpa Throws and Blankets Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Sold on Amazon by OCTROT

The electrical cord on the recalled throws and blankets can detach and ignite, posing a risk of serious injury or death from fire, burn and shock hazards.

Jul 30, 2026
Safety AlertUSCPSC

Golden Link Recalls Fantastic Four Cups and Captain America Popcorn Helmet Containers with LED Lights Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Mandatory Standard for Consumer Products with Button Cell Batteries

Unknown Firm
Golden Link Recalls Fantastic Four Cups and Captain America Popcorn Helmet Containers with LED Lights Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
CPSCGeneral Alert

Golden Link Recalls Fantastic Four Cups and Captain America Popcorn Helmet Containers with LED Lights Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Mandatory Standard for Consumer Products with Button Cell Batteries

The cups and containers violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. In addition, the products do not bear the warning labels required by Reese's Law. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.

Jul 30, 2026
Vehicle RecallUSNHTSA

Wanco, Inc. - Fuel Tank May Crack and Leak

Wanco, Inc.
NHTSAFUEL SYSTEM, DI...

Wanco, Inc. - Fuel Tank May Crack and Leak

A fuel leak in the presence of an ignition source increases the risk of a fire.

Jul 30, 2026Wanco, Inc.
Safety AlertUSCPSC

HARPPA Recalls Nordi Toddler Tower Stools Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards

Unknown Firm
HARPPA Recalls Nordi Toddler Tower Stools Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards
CPSCGeneral Alert

HARPPA Recalls Nordi Toddler Tower Stools Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards

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 death due to tip over, fall and entrapment hazards.

Jul 30, 2026
Vehicle RecallUSNHTSA

Brinkley RV - Exterior Ladder May Detach

Brinkley RV
NHTSASTRUCTURE

Brinkley RV - Exterior Ladder May Detach

The ladder may detach during use, increasing the risk of injury.

Jul 30, 2026Brinkley RV
Safety AlertUSCPSC

Galanz Americas Recalls Retro Refrigerators Due to Risk of Serious Injury or Death from Fire and Burn Hazards; One Death Reported

Zhongshan Galanz, of China
Galanz Americas Recalls Retro Refrigerators Due to Risk of Serious Injury or Death from Fire and Burn Hazards; One Death Reported
CPSCGeneral Alert

Galanz Americas Recalls Retro Refrigerators Due to Risk of Serious Injury or Death from Fire and Burn Hazards; One Death Reported

The recalled refrigerators' internal electrical components can short circuit and ignite, posing a risk of serious injury or death from fire and burn hazards.

Jul 30, 2026Zhongshan Galanz, of China
Vehicle RecallUSNHTSA

Chrysler (FCA US, LLC) - Improperly Installed Seat Belt Buckle Anchor/FMVSS 210

Chrysler (FCA US, LLC)
NHTSASEAT BELTS

Chrysler (FCA US, LLC) - Improperly Installed Seat Belt Buckle Anchor/FMVSS 210

An improperly installed seat belt buckle anchor may fail to properly restrain occupants, increasing the risk of injury during a crash.

Jul 30, 2026Chrysler (FCA US, LLC)
Medical DeviceUSFDA Devices

FARASTAR PFA Generator, Product ID M004PFCE61M460; Percutaneous Cardiac Ablation Catheter

Boston Scientific Corporation
FDA DevicesClass II

FARASTAR PFA Generator, Product ID M004PFCE61M460; Percutaneous Cardiac Ablation Catheter

Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information.

Jul 29, 2026Boston Scientific Corporation
Medical DeviceUSFDA Devices

Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 20 mm 027 REF PED2-300-20

Micro Therapeutics, Inc.
FDA DevicesClass II

Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 20 mm 027 REF PED2-300-20

Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20 mm implants.

Jul 29, 2026Micro Therapeutics, Inc.
Medical DeviceUSFDA Devices

Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.

AVID Medical, Inc.
FDA DevicesClass II

Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.

Incorrect concentration of Betadine solution contained within certain AVID convenience kits.

Jul 29, 2026AVID Medical, Inc.
Medical DeviceUSFDA Devices

SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.

KENT IMAGING, INC.
FDA DevicesClass II

SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.

The software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a battery that has fully discharged into a low-power "shipping mode." When this occurs, an affected device will not resume charging when reconnected to power and becomes temporarily unusable/ unavailable for wound imaging until corrected.

Jul 29, 2026KENT IMAGING, INC.
PharmaceuticalUSFDA Drugs

Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 90, 0.2%), Sterile 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310742011012, NDC 10742-8158-1

Rohto-Mentholatum (Vietnam) Co., Ltd.
FDA DrugsClass II

Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 90, 0.2%), Sterile 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310742011012, NDC 10742-8158-1

Lack of Assurance of Sterility

Jul 29, 2026Rohto-Mentholatum (Vietnam) Co., Ltd.
Medical DeviceUSFDA Devices

Ventriculostomy Kit, REF: 46154

Medtronic Neurosurgery
FDA DevicesClass II

Ventriculostomy Kit, REF: 46154

Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the acceptable limit for devices that come into contact with cerebrospinal fluid; endotoxin exposure can cause an acute inflammatory process.

Jul 29, 2026Medtronic Neurosurgery
Medical DeviceUSFDA Devices

MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G

Medline Industries, LP
FDA DevicesClass I

MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G

Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. B. Braun Medical Inc. was notified by their supplier, Spectra Medical Devices, LLC of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. Huons Co, Ltd. has issued a voluntary recall of this product due to quality issues.

Jul 29, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116I

Medline Industries, LP
FDA DevicesClass II

Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116I

Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of urinary catheters that exhibit staining on the catheter surface; raw material present in increased amounts may be harmful.

Jul 29, 2026Medline Industries, LP

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