États-Unis Recalls

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

Showing 24 of 17,563 results
Safety AlertUSCPSC

Vndueey Magnetic Men Toy Sets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys

Unknown Firm
Vndueey Magnetic Men Toy Sets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
CPSCGeneral Alert

Vndueey Magnetic Men Toy Sets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys

The recalled magnetic stick figure toy sets violate the mandatory standard for toys because the sets contain loose magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, they can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

Jan 22, 2026
Safety AlertUSCPSC

Yetonamr Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Longyanguiheng

Unknown Firm
Yetonamr Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Longyanguiheng
CPSCGeneral Alert

Yetonamr Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Longyanguiheng

The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller than permitted. The silicone strings can reach the back of the throat and become lodged, posing a risk of respiratory distress, serious choking hazard and death.

Jan 22, 2026
Safety AlertUSCPSC

Based Online Fidget Magnet Ball Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys

Unknown Firm
Based Online Fidget Magnet Ball Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
CPSCGeneral Alert

Based Online Fidget Magnet Ball Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys

The magnet ball toys violate the mandatory standard for toys because they are loose high-powered magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, they can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

Jan 22, 2026
Safety AlertUSCPSC

Thrasio Recalls Angry Orange Enzyme Stain Removers Due to Risk of Exposure to Bacteria

Unknown Firm
Thrasio Recalls Angry Orange Enzyme Stain Removers Due to Risk of Exposure to Bacteria
CPSCGeneral Alert

Thrasio Recalls Angry Orange Enzyme Stain Removers Due to Risk of Exposure to Bacteria

The recalled products can contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened immune systems, external medical devices, or underlying lung conditions who are exposed to Pseudomonas aeruginosa face a risk of serious infection that may require medical treatment. The bacteria can enter the body if inhaled, through the eyes, or through a break in the skin. People with healthy immune systems are usually not affected by bacteria.

Jan 22, 2026
Safety AlertUSCPSC

Gagaku Children's Ice Cream Toy Playsets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion Hazard; Violate Mandatory Standard for Toys; Sold on Amazon by Brandworl.USA

Unknown Firm
Gagaku Children's Ice Cream Toy Playsets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion Hazard; Violate Mandatory Standard for Toys; Sold on Amazon by Brandworl.USA
CPSCGeneral Alert

Gagaku Children's Ice Cream Toy Playsets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion Hazard; Violate Mandatory Standard for Toys; Sold on Amazon by Brandworl.USA

The recalled toys violate the mandatory standard for toys because they contain high-powered magnets which can loosen and detach, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting and/or blockage of the intestines, blood poisoning and death.

Jan 22, 2026
Safety AlertUSCPSC

Iristar Minoxidil Spray Bottles for Hair and Beard Growth Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Moralowen

Shaoshan Leiluo Trading Co., Ltd. of Shaoshan, Hunan of China
Iristar Minoxidil Spray Bottles for Hair and Beard Growth Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Moralowen
CPSCGeneral Alert

Iristar Minoxidil Spray Bottles for Hair and Beard Growth Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Moralowen

The recalled spray bottles contain minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.

Jan 22, 2026Shaoshan Leiluo Trading Co., Ltd. of Shaoshan, Hunan of China
Safety AlertUSCPSC

Aborder Products Recalls Cumbor Retractable Safety Gates Due to Risk of Serious Injury or Death to Children from Entrapment; Violates Mandatory Standard for Gates and Enclosures

Unknown Firm
Aborder Products Recalls Cumbor Retractable Safety Gates Due to Risk of Serious Injury or Death to Children from Entrapment; Violates Mandatory Standard for Gates and Enclosures
CPSCGeneral Alert

Aborder Products Recalls Cumbor Retractable Safety Gates Due to Risk of Serious Injury or Death to Children from Entrapment; Violates Mandatory Standard for Gates and Enclosures

The recalled gates violate the mandatory standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the gate and the floor, posing a risk of serious injury or death due to entrapment.

Jan 22, 2026
Safety AlertUSCPSC

Topkay Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Multipurpose Lighters; Sold on Amazon by Xiyude

Unknown Firm
Topkay Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Multipurpose Lighters; Sold on Amazon by Xiyude
CPSCGeneral Alert

Topkay Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Multipurpose Lighters; Sold on Amazon by Xiyude

The recalled lighters violate the mandatory standard for multipurpose lighters because they do not have the required child-resistant mechanisms, posing a risk of serious injury or death from fire and burn hazards.

Jan 22, 2026
Vehicle RecallUSNHTSA

Blue Bird Body Company - Illegible DOT Marking on Window/FMVSS 205

Blue Bird Body Company
NHTSAVISIBILITY

Blue Bird Body Company - Illegible DOT Marking on Window/FMVSS 205

A missing DOT code mark may result in the window being replaced with an incorrect type of glass, increasing the risk of a injury.

Jan 22, 2026Blue Bird Body Company
Vehicle RecallUSNHTSA

General Motors, LLC - Damaged Parking Brake Wiring Harness

General Motors, LLC
NHTSAGeneral Alert

General Motors, LLC - Damaged Parking Brake Wiring Harness

Unintended activation of the parking brake while driving increases the risk of a crash. Loss of the parking brake function while parked can result in a rollaway, increasing the risk of a crash.

Jan 22, 2026General Motors, LLC
Vehicle RecallUSNHTSA

Blue Bird Body Company - Illegible DOT Marking on Window/FMVSS 205

Blue Bird Body Company
NHTSAVISIBILITY

Blue Bird Body Company - Illegible DOT Marking on Window/FMVSS 205

A missing DOT code mark may result in the window being replaced with an incorrect type of glass, increasing the risk of a injury.

Jan 22, 2026Blue Bird Body Company
Safety AlertUSCPSC

Academy Sports + Outdoors Recalls Magellan Odyssey Rocker Chairs Due to Injury and Fall Hazards

Unknown Firm
Academy Sports + Outdoors Recalls Magellan Odyssey Rocker Chairs Due to Injury and Fall Hazards
CPSCGeneral Alert

Academy Sports + Outdoors Recalls Magellan Odyssey Rocker Chairs Due to Injury and Fall Hazards

The recalled chairs' legs can break, posing injury and fall hazards to consumers.

Jan 22, 2026
Safety AlertUSCPSC

Johnson Health Tech Expands Recall to Include Matrix Retail and Vision Treadmills Due to Fire Hazard

Unknown Firm
Johnson Health Tech Expands Recall to Include Matrix Retail and Vision Treadmills Due to Fire Hazard
CPSCGeneral Alert

Johnson Health Tech Expands Recall to Include Matrix Retail and Vision Treadmills Due to Fire Hazard

The power cord can become loose from the treadmill's power socket, posing a fire hazard.

Jan 22, 2026
PharmaceuticalUSFDA Drugs

Benadryl, 25'S 2PK Box, UPC 815556020316

GOLD STAR DISTRIBUTION INC
FDA DrugsClass II

Benadryl, 25'S 2PK Box, UPC 815556020316

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Jan 21, 2026GOLD STAR DISTRIBUTION INC
Food & BeverageUSFDA Food

Healthy Truth brand Moringa Powder; 5lb and 20lb

Organic Living Superfoods Llc
FDA FoodClass I

Healthy Truth brand Moringa Powder; 5lb and 20lb

Products may be contaminated with Salmonella Richmond.

Jan 21, 2026Organic Living Superfoods Llc
PharmaceuticalUSFDA Drugs

Lanreotide Injection, 120 mg/0.5 mL, 0.5 mL per pre-filled syringe, For deep subcutaneous injection, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-870-67

Cipla USA, Inc.
FDA DrugsClass II

Lanreotide Injection, 120 mg/0.5 mL, 0.5 mL per pre-filled syringe, For deep subcutaneous injection, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-870-67

Presence of Particulate Matter.

Jan 21, 2026Cipla USA, Inc.
Medical DeviceUSFDA Devices

Allura Xper FD10; Model Number: 722003;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Allura Xper FD10; Model Number: 722003;

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.

Jan 21, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
PharmaceuticalUSFDA Drugs

Claritin, 20 Count, UPC: 655708016305

GOLD STAR DISTRIBUTION INC
FDA DrugsClass II

Claritin, 20 Count, UPC: 655708016305

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Jan 21, 2026GOLD STAR DISTRIBUTION INC
Food & BeverageUSFDA Food

Atwater's, Holiday Cookie Tin, 19.65 ounces, Round metal tin with a window lid

One Roof LLC
FDA FoodClass I

Atwater's, Holiday Cookie Tin, 19.65 ounces, Round metal tin with a window lid

Undeclared tree nut allergens: almonds, pecans, and walnuts.

Jan 21, 2026One Roof LLC
Food & BeverageUSFDA Food

Brussel Sprouts & Kale Slaw

WFM Purchasing, LP
FDA FoodClass I

Brussel Sprouts & Kale Slaw

Undeclared Fish and Egg Allergen

Jan 21, 2026WFM Purchasing, LP
Medical DeviceUSFDA Devices

Allura Xper FD10F; Model Number: 722002;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Allura Xper FD10F; Model Number: 722002;

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.

Jan 21, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
PharmaceuticalUSFDA Drugs

LIQUID NYQUIL a) regular, 12/8oz; b) cherry, 12/8oz

GOLD STAR DISTRIBUTION INC
FDA DrugsClass II

LIQUID NYQUIL a) regular, 12/8oz; b) cherry, 12/8oz

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Jan 21, 2026GOLD STAR DISTRIBUTION INC
PharmaceuticalUSFDA Drugs

AQ 120 GFEW, Aquarion Preserved Cartridges (2) 3.7 Gallons each

Encon Safety Products Co
FDA DrugsClass II

AQ 120 GFEW, Aquarion Preserved Cartridges (2) 3.7 Gallons each

cGMP deviations.

Jan 21, 2026Encon Safety Products Co
Food & BeverageUSFDA Food

HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4

Herbs Forever
FDA FoodClass I

HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4

Potential undeclared allergen ingredient (Wheat)

Jan 21, 2026Herbs Forever

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