Estados Unidos Recalls

Retiros de seguridad del consumidor de la FDA, CPSC, NHTSA y USDA FSIS.

Showing 24 of 17,562 results
Vehicle RecallUSNHTSA

Magic Tilt Trailers, Inc. - Weld Failure May Allow Winch to Detach

Magic Tilt Trailers, Inc.
NHTSAEQUIPMENT

Magic Tilt Trailers, Inc. - Weld Failure May Allow Winch to Detach

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

Aug 28, 2026Magic Tilt Trailers, Inc.
Vehicle RecallUSNHTSA

Jayco, Inc. - Incorrect GAWR on Certification Label

Jayco, Inc.
NHTSAEQUIPMENT

Jayco, Inc. - Incorrect GAWR on Certification Label

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

Aug 28, 2026Jayco, Inc.
Safety AlertUSRSS Feed

Everything Sprouts, LLC Expands Voluntarily Recall to Include Robust Radish Mix Due to Potential E. Coli and Salmonella Risk

Unknown Firm
RSS FeedGeneral Alert

Everything Sprouts, LLC Expands Voluntarily Recall to Include Robust Radish Mix Due to Potential E. Coli and Salmonella Risk

Aug 28, 2026
Safety AlertUSRSS Feed

Panorama Produce Recalls Mangoes Due to Possible Salmonella Contamination

Unknown Firm
RSS FeedGeneral Alert

Panorama Produce Recalls Mangoes Due to Possible Salmonella Contamination

Aug 28, 2026
Vehicle RecallUSNHTSA

Altec Industries, Inc. - Strobe Light May Short Circuit

Altec Industries, Inc.
NHTSAEQUIPMENT

Altec Industries, Inc. - Strobe Light May Short Circuit

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

Aug 27, 2026Altec Industries, Inc.
Safety AlertUSRSS Feed

Ana Salazar Modela Tu Cuerpo Inc. Issues Nationwide Voluntary Recall of Lipofit Extreme Fat Burner 2.0 Due to Presence of Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Unknown Firm
RSS FeedGeneral Alert

Ana Salazar Modela Tu Cuerpo Inc. Issues Nationwide Voluntary Recall of Lipofit Extreme Fat Burner 2.0 Due to Presence of Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Aug 27, 2026
Safety AlertUSRSS Feed

B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container Due to the Presence of Particulate Matter

Unknown Firm
RSS FeedGeneral Alert

B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container Due to the Presence of Particulate Matter

Aug 27, 2026
Safety AlertUSCPSC

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

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

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 or death from choking and ingestion hazards.

Aug 27, 2026
Safety AlertUSCPSC

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

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

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 hazard.

Aug 27, 2026
Safety AlertUSCPSC

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

Unknown Firm
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
CPSCGeneral Alert

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

Aug 27, 2026
Safety AlertUSCPSC

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

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

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 electrocution hazards.

Aug 27, 2026
Safety AlertUSCPSC

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

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

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 electrocution hazards.

Aug 27, 2026
Safety AlertUSCPSC

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

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

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.

Aug 27, 2026
Safety AlertUSCPSC

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

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

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.

Aug 27, 2026
Safety AlertUSCPSC

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

Diamond Wipes International, Inc., of Chino, California
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
CPSCGeneral Alert

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 child-resistant, posing a risk of serious injury or death from poisoning if the contents of the wipes are ingested by young children.

Aug 27, 2026Diamond Wipes International, Inc., of Chino, California
Safety AlertUSCPSC

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

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

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.

Aug 27, 2026
Safety AlertUSCPSC

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

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

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.

Aug 27, 2026
Safety AlertUSCPSC

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

Unknown Firm
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
CPSCGeneral Alert

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 silicone strings can reach the back of children’s throat and become lodged, posing a risk of respiratory distress and deadly choking hazard.

Aug 27, 2026
Vehicle RecallUSNHTSA

Bell Sports, Inc. - Helmets with Inadequate Impact Protection/FMVSS 218

Bell Sports, Inc.
NHTSAEQUIPMENT

Bell Sports, Inc. - Helmets with Inadequate Impact Protection/FMVSS 218

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

Aug 26, 2026Bell Sports, Inc.
Food & BeverageUSFDA Food

Whole Foods Mango Pineapple Salsa sold as a condiment in Caribbean Mango Pineapple Turkey Burger. Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is applied. Products contain the following PLU Cods located under label bar code: 25867600000, 21195900000, 46000040275, 27578600000. Packed for Whole Foods Market, 4301 W. William Cannon, Austin, TX 78749.

WFM Purchasing, LP
FDA FoodClass I

Whole Foods Mango Pineapple Salsa sold as a condiment in Caribbean Mango Pineapple Turkey Burger. Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is applied. Products contain the following PLU Cods located under label bar code: 25867600000, 21195900000, 46000040275, 27578600000. Packed for Whole Foods Market, 4301 W. William Cannon, Austin, TX 78749.

Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.

Aug 26, 2026WFM Purchasing, LP
Medical DeviceUSFDA Devices

One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device.

Intersurgical Inc
FDA DevicesClass II

One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device.

Devices could potentially be occluded or partially occluded.

Aug 26, 2026Intersurgical Inc
Food & BeverageUSUSDA FSIS

Shanghai Ravioli Corporation Recalls Not Ready-To-Eat Frozen Buffalo Chicken Products Produced Without the Benefit of Inspection

Unknown Firm
USDA FSISClass I

Shanghai Ravioli Corporation Recalls Not Ready-To-Eat Frozen Buffalo Chicken Products Produced Without the Benefit of Inspection

Produced Without Benefit of Inspection

Aug 26, 2026
Medical DeviceUSFDA Devices

Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001

Paragonix Technologies Inc.
FDA DevicesClass II

Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001

Due to a firmware defect, the portable organ transfer device datalogger may lose its configuration, resulting in a blank screen and loss of displayed preservation parameters.

Aug 26, 2026Paragonix Technologies Inc.
Safety AlertUSRSS Feed

Revival Animal Health, LLC Voluntarily Recalls Feline Milk Replacers Due to Inconsistent Levels of Vitamins and Trace Minerals

Unknown Firm
RSS FeedGeneral Alert

Revival Animal Health, LLC Voluntarily Recalls Feline Milk Replacers Due to Inconsistent Levels of Vitamins and Trace Minerals

Aug 26, 2026

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