Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

9326–9350 of 113902

ModerateFDA (Devices)·Z-1744-2025·2025-05-21
Contour Gold Eyelid Weight implants recalled for mislabeling
Meddev Corp is recalling Contour Gold Eyelid Weight implants (Model LL3010, 1.0 gm) due to mislabeling. The recall affects 34 units distributed nationwide across 17 states.
Product
Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3010 Product Description: Contour Gold Eyelid Weight, 1.0 gm MedDev Contour and ThinProfile Eyelid Weight Implants are designed for the gravity-assisted treatment of protracted permanent
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0788-2025·2025-05-21
Johnny Rockets Vanilla Flavored Ice Cream Recalled for Plastic Contamination
Wells Enterprises is recalling Johnny Rockets Vanilla Flavored Ice Cream (3-gallon tubs) because plastic material may be present in the product.
Product
Johnny Rockets Vanilla Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640006564, Item: 902486
Category
Food
Distribution
0 states
ModerateFDA (Food)·F-0785-2025·2025-05-21
GFGB Vanilla Bean Flavored Ice Cream recalled for plastic contamination
Wells Enterprises is recalling GFGB Vanilla Bean Flavored Ice Cream in 3-gallon tubs because plastic material may be present in the product.
Product
GFGB Vanilla Bean Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640000272, Item: 669740
Category
Food
Distribution
0 states
ModerateFDA (Food)·F-0779-2025·2025-05-21
Rocky Road Flavored Ice Cream recalled for possible plastic contamination
Wells Enterprises is recalling Rocky Road Flavored Ice Cream 3-gallon tubs due to possible plastic material in the product. The affected ice cream was distributed to over 100 distribution centers across the United States.
Product
Rocky Road Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640050314, Item: 19695
Category
Food
Distribution
0 states
ModerateFDA (Food)·F-0784-2025·2025-05-21
Cotton Candy Flavored Ice Cream recalled for possible plastic contamination
Wells Enterprises is recalling Cotton Candy Flavored Ice Cream 3-gallon tubs because foreign plastic material may be present in the product.
Product
Cotton Candy Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640050482, Item: 662429
Category
Food
Distribution
0 states
ModerateFDA (Food)·F-0799-2025·2025-05-21
Keith Valley Vanilla Flavored Ice Cream Recalled for Possible Plastic
Wells Enterprises is recalling Keith Valley Vanilla Flavored Ice Cream 3-gallon tubs due to the possible presence of plastic foreign material in the product.
Product
Keith Valley Vanilla Flavored Ice Cream, 3 GAL, DISTRIBUTED BY Ben E. Keith Foods, Fort Worth, TX 76101 UPC: 046045065871, Item: 1144343
Category
Food
Distribution
0 states
ModerateFDA (Food)·F-0797-2025·2025-05-21
Glenview Farms French Vanilla Ice Cream Recalled for Plastic Contamination
Glenview Farms Artificially Flavored French Vanilla Ice Cream in 3-gallon tubs is being recalled because plastic material may be present in the product. Consumers should not consume the product.
Product
Glenview Farms Artificially Flavored French Vanilla Ice Cream, 3 GAL, DISTRIBUTED BY US FOODS, INC, Rosemont, IL 60018, UPC: 50758108392668, Item: 785887
Category
Food
Distribution
0 states
ModerateFDA (Devices)·Z-1753-2025·2025-05-21
PiezoWave 2 Control Unit therapeutic massager high voltage capacitor failure
Richard Wolf GmbH is recalling 31 PiezoWave 2 Control Units (Product Number 100506US) due to a high voltage capacitor that may fail early in the device's life cycle, potentially producing smoke, burning smell, spark, or excessive heat.
Product
PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric shockwaves (Therapeutic massager).
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-1761-2025·2025-05-21
Augmedics Perc Pin Adaptor component recalled due to design defect
Augmedics Ltd. is recalling the Perc Pin Adaptor, a component of the xvision Spine surgical navigation system, because the tightening knob is inconvenient to use and the tightening markings are improperly placed.
Product
Augmedics Perc Pin Adaptor, Model/Catalog Number AMCH07200, a component of the xvision Spine (XVS) system, an image-guided navigation system that is designed to assist surgeons in placing pedicle screws accurately, during open or percutaneous computer-assisted spinal surgery.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1764-2025·2025-05-21
CMS8000 Patient Monitor Has Nine Cybersecurity Vulnerabilities
The CMS8000 Patient Monitor manufactured by Contec Medical Systems Co., Ltd. has nine identified cybersecurity vulnerabilities. The FDA is issuing this Class II recall affecting approximately 7,773 units distributed nationwide.
Product
CMS8000 Patient Monitor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1784-2025·2025-05-21
Beckman Coulter DxC 500 AU Chemistry Analyzer Software Calibration Error
Beckman Coulter is recalling the DxC 500 AU Clinical Chemistry Analyzer due to a software error that prevents the analyzer from completing calibration orders under certain conditions, which can delay test result reporting.
Product
DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065. The Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer is an automated chemistry analyzer that measures analytes in samples, in combination with appropriat
Category
Medical Device
Distribution
17 states
ModerateFDA (Food)·F-0798-2025·2025-05-21
Wells Enterprises French Vanilla Ice Cream Recalled for Plastic Contamination
Wells Enterprises is recalling 17 3-gallon tubs of Artificially Flavored French Vanilla Ice Cream distributed by Sysco Corporation because plastic material may be present in the product.
Product
Artificially Flavored French Vanilla Ice Cream, 3 GAL, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TX 77077UPC: 00074865257275, Item: 1026416
Category
Food
Distribution
0 states
ModerateFDA (Drugs)·D-0417-2025·2025-05-21
La Roche-Posay Effaclar Duo Acne Treatment Recalled for Benzene Contamination
La Roche-Posay Effaclar Duo acne treatment is being recalled due to detected trace levels of benzene. The recall affects 2,226,801 units distributed nationwide.
Product
La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, 40 mL (135 FL. OZ.) Tube per carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, Laboratoire Dermatologique, CAI 86270, La Roche-
Category
Drug
Distribution
Distributed nationwide
SevereUSDA FSIS·017-2025·2025-05-20
Snack Mania Recalls Uninspected Frozen Chicken Coxinhas Products
Snack Mania Brazilian Delights Corp. is recalling approximately 9,722 pounds of frozen chicken coxinhas produced without federal inspection. No illnesses have been reported.
Product
Snack Mania Brazilian Delights Corp., Recalls Ready-To-Eat Chicken Coxinhas Products Produced Without Benefit of Inspection
Category
Food
Distribution
1 state
SevereUSDA FSIS·016-2025·2025-05-20
Bourgeois Smokehouse Recalls Smoked Andouille Sausage Due to Listeria
Bourgeois Smokehouse is recalling approximately 100 pounds of ready-to-eat smoked andouille sausage sold in Alabama, Louisiana, and Mississippi due to possible Listeria monocytogenes contamination.
Product
Bourgeois Smokehouse Recalls Ready-To-Eat Smoked Andouille Sausage Products Due to Possible Listeria Contamination
Category
Food
Distribution
1 state
HighNHTSA·25V327000·2025-05-20
Braun Recalls Demers Ambulances Due to Unsecured Cushion Equipment Storage
Braun Industries is recalling specific Demers ambulance models because improperly installed cushion equipment storage may allow items to detach during transit, increasing injury risk.
Product
DEMERS — DEMERS, DEMERS AMBULANCES TSE, TXE, MX164E, MXP150E
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V328000·2025-05-20
Orange EV Recalls Electric Trucks Due to Obstructed Backup Lights
Orange EV is recalling specific electric trucks because a pintle hook blocks the backup lights, reducing visibility and increasing crash risk.
Product
ORANGE EV — ORANGE EV E-TRIEVER, HUSK-E, T-SERIES ELECTRIC TRUCK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25T008000·2025-05-19
Michelin Recalls Agilis Cross Climate Tires Due to Tread Rubber Detachment
Michelin is recalling specific Agilis Cross Climate tires because chunks of tread rubber may detach, increasing the risk of tire failure and a crash.
Product
TIRES:TREAD/BELT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V319000·2025-05-16
Isuzu Recalls 2025 NRR EV Due to Electrical Overheating Risk
Isuzu is recalling 2025 NRR EV vehicles because a gap in the electrical system may cause overheating and loss of drive power, increasing crash risk.
Product
ISUZU — ISUZU NRR EV
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·015-2025·2025-05-16
USDA recalls Fijian Import & Export ready-to-eat meat pie products
Fijian Import & Export Co. Inc. is recalling approximately 127 pounds of ready-to-eat meat pie products imported from Australia that were not presented for FSIS import reinspection. The products were shipped to Rutter's convenience stores in Pennsylvania.
Product
Fijian Import & Export Co. Inc. Recalls Ready-To-Eat Meat Pie Products Imported Without Benefit of Import Reinspection
Category
Food
Distribution
1 state
CriticalCPSC·25285·2025-05-15
Chill Pill Magnetic Haptic Fidget Toys recalled due to ingestion hazard
FidgetThings is recalling Chill Pill Magnetic Haptic Fidget Toys Red Bumpy because they violate federal magnet regulations and pose a risk of serious injury or death if swallowed by children.
Product
Chill Pill Magnetic Haptic Fidget Toys Red Bumpy
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25286·2025-05-15
Child Safety Gates Recalled for Entrapment and Fall Hazards
Multiple child safety gates sold on Amazon.com violate federal safety regulations, posing risk of serious injury or death from entrapment and falls. Consumers should stop using the gates immediately and contact the seller for disposal and refund.
Product
Child Safety Gates
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25279·2025-05-15
NICREW Submersible RGB LED Lights Recalled for Coin Battery Ingestion Hazard
NICREW 15" Submersible RGB LED Lights with remote controls are recalled because the remote's lithium coin battery can be easily accessed by children, creating a serious ingestion hazard that can cause internal burns and death.
Product
NICREW 15" Submersible RGB LED Lights with remote controls
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25280·2025-05-15
Digital Wall Clocks recalled for ingestion hazard from coin battery
Leon Rading Co. Ltd. is recalling digital wall clocks (model PH-05) sold on Amazon because the remote control contains a lithium coin battery that children can easily access and swallow, risking serious internal injury or death.
Product
Digital Wall Clocks
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25281·2025-05-15
PlayTab Rollers Tile Toys Recalled for Magnet Ingestion Hazard
Fat Brain Toy Co. is recalling PlayTab Rollers Tile Toys because they contain magnets that can become loose and be swallowed by children, posing a risk of serious injury or death.
Product
PlayTab Rollers Tile Toys
Category
Consumer Product
Distribution
Distributed nationwide

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9326–9350 of 113902