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

7101–7125 of 89525

HighFDA (Devices)·Z-1749-2025·2025-05-21
Abbott Alinity m Resp-4-Plex AMP Kit Multiplex PCR Test Recall
Abbott Molecular is recalling the Alinity m Resp-4-Plex AMP Kit (List Number 09N79-096) due to reports of increased reactive negative controls and false positive results in respiratory viral testing.
Product
Alinity m Resp-4-Plex AMP Kit, List Number 09N79-096, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended for the simultaneous qualitative detection and differentiation of RNA from SARS-CoV-2, influenza A virus (flu A), influenza B virus
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V334000·2025-05-21
Volkswagen Atlas rearview camera image can become distorted in reverse
Volkswagen is recalling certain 2024-2025 Atlas and Atlas Cross Sport vehicles because a software error may distort the rearview camera image when the vehicle is in reverse.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0769-2025·2025-05-21
Bonya Raspberry Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Raspberry Yogurt Parfait (8oz) because it contains undeclared almonds, which pose an allergy risk. The recall affects 6,984 units distributed to NY, PA, MA, and NJ.
Product
Bonya Raspberry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-1778-2025·2025-05-21
Philips Intera 1.5T MRI Scanner QBC Seal Adhesive Failure Risk
Philips is recalling the Intera 1.5T Power/Pulsar MRI scanner because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
Intera 1.5T Power/Pulsar, Model Number: 781105;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1773-2025·2025-05-21
Philips Intera 1.0T MRI Quadrature Body Coil Seal Failure Recall
Philips is recalling Intera 1.0T Power/Pulsar MRI systems (Model 781103) due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and injure patients during scanning.
Product
Intera 1.0T Power/Pulsar, Model Number: 781103;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V330000·2025-05-21
Ram ProMaster rearview camera image may not display in reverse
Chrysler is recalling certain 2022-2025 Ram ProMaster vehicles because a software error in the security gateway module may prevent the rearview camera image displaying, failing FMVSS 111.
Product
RAM — RAM, BRAUN PROMASTER, RAM PROMASTER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1777-2025·2025-05-21
Philips Intera 1.5T MRI Scanner Quadrature Body Coil Seal Failure
Philips is recalling the Intera 1.5T Omni/Stellar MRI scanner due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and cause patient injury. The loose seal during scanning could result in skin abrasions, bruises, lacerations, hair loss, or tissue damage.
Product
Intera 1.5T Omni/Stellar, Model Number: 781104;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1772-2025·2025-05-21
Philips Intera 1.0T MRI System Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.0T Omni/Stellar MRI systems (37 units: 3 in US, 34 internationally) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that can cause skin injuries during patient scanning.
Product
Intera 1.0T Omni/Stellar, Model Number: 781102;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1780-2025·2025-05-21
Philips Intera 3.0T Quasar Dual MRI Scanner Coil Seal Adhesive Failure
Philips is recalling the Intera 3.0T Quasar Dual MRI scanner (Model 781150) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
Intera 3.0T Quasar Dual, Model Number: 781150;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1781-2025·2025-05-21
Philips Intera CV MRI Quadrature Body Coil Seal Adhesive Failure Recall
Philips is recalling Intera CV MRI units (Model 781107) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning, including skin abrasions, lacerations, or tissue damage.
Product
Intera CV, Model Number: 781107;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1779-2025·2025-05-21
Philips Intera 1.5T R11 MRI System Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.5T R11 MRI systems because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could contact patients and cause skin injuries.
Product
Intera 1.5T R11, Model Number: 781170;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V333000·2025-05-21
Mack Recalls 2026 MD Trucks Due to Incorrect Seat Belt Routing
Mack Trucks is recalling 2026 MD vehicles because the center bench seat belt assembly may be routed incorrectly, potentially failing to restrain occupants in a crash.
Product
MACK — MACK MD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25E036000·2025-05-21
Holley Recalls Fuel Pressure Regulators Due to Leak Risk
Holley Performance Products is recalling specific Fuel Pressure Regulators because a damaged diaphragm may cause a fuel leak, increasing the risk of fire.
Product
FUEL SYSTEM, GASOLINE recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0778-2025·2025-05-21
President Brand Kumquat Slices Recalled for Undeclared Sulfites
East CK Trading Inc. is recalling President Brand Kumquat Slices because they contain undeclared sulfites. Sulfites are a known allergen that can cause serious reactions in sensitive individuals.
Product
PRESIDENT BRAND; Kumquat Slices; NET WT. 8 OZ/227g; EAST CK TRADING INC.; INGREDIENTS: Kumquat slices; packaged in clear plastic jars with UPC 8 10077 20936 3
Category
Food
Distribution
4 states
HighFDA (Food)·F-0804-2025·2025-05-21
Blueberry Lemon Scones recalled for undeclared soy allergen
The Hot Chocolatier - St. Elmo, LLC is recalling Blueberry Lemon Scones sold in bulk bakery boxes because they contain undeclared soy, a common allergen.
Product
Blueberry Lemon Scones, bulk packaged in bakery boxes. Products are sold at retail in pastry cases and not individually labeled.
Category
Food
Distribution
1 state
HighFDA (Food)·F-0783-2025·2025-05-21
Scooper Hero Ice Cream recalled for possible plastic contamination
Wells Enterprises is recalling Scooper Hero Ice Cream 3-gallon tubs because plastic foreign material may be present in the product.
Product
Scooper Hero Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640050642, Item: 487054
Category
Food
Distribution
0 states
HighFDA (Food)·F-0790-2025·2025-05-21
Vanilla Frozen Yogurt Recalled for Possible Plastic Foreign Material
Wells Enterprises is recalling Vanilla Frozen Yogurt 3-gallon tubs due to the possible presence of plastic material in the product.
Product
Vanilla Frozen Yogurt, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 00070640022144, Item: 1352604
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1782-2025·2025-05-21
Philips SmartPath dStream 1.5T MRI coil may create sharp edges
Philips is recalling SmartPath to dStream 1.5T MRI units (Model 782146) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could cause skin abrasions, lacerations, or tissue injury to patients.
Product
SmartPath to dStream for 1.5T, Model Number: 782146;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1743-2025·2025-05-21
Halyard RAPIDES E-PACK Cardiovascular Procedure Kit Surgical Needle Coating Issue
AVID Medical is recalling Halyard RAPIDES E-PACK Cardiovascular Procedure Convenience Kits due to a raw material defect in surgical needle coating that may cause diminished performance or coating removal during use.
Product
Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0792-2025·2025-05-21
Wells Dairy GFGB Vanilla Ice Cream Recalled for Plastic Contamination
Wells Enterprises is recalling GFGB 12% Vanilla Flavored Ice Cream (3-gallon tubs) because plastic foreign material may be present in the product. Consumers should not consume the product and should contact the company or retailer.
Product
GFGB 12% Vanilla Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640018451, Item: 1435313
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1776-2025·2025-05-21
Philips Intera 1.5T MRI Scanner Body Coil Seal Failure Recall
Philips is recalling 103 Intera 1.5T MRI scanners worldwide because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could cause skin abrasions, bruises, lacerations, hair loss, or tissue injury to patients.
Product
Intera 1.5T Master/Nova, Model Number: 781106;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0787-2025·2025-05-21
Planet Smoothie Frozen Yogurt Recalled for Possible Plastic Foreign Material
Wells Enterprises is recalling Planet Smoothie ZSA Vanilla Flavored Fat Free Frozen Yogurt (3-gallon tubs) because plastic foreign material may be present in the product.
Product
Planet Smoothie ZSA Vanilla Flavored Fat Free Frozen Yogurt, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640005567, Item: 889334
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1769-2025·2025-05-21
KliniTray Platte Faxitron Sterile Tissue Resection Examination Board Recalled
KliniTray Platte Faxitron sterile tissue resection margin examination boards (Model 2001155-F) are being recalled due to potential for microbial contamination. Affected units were distributed nationwide.
Product
KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact
Category
Medical Device
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

How to read this listing

Filters

7101–7125 of 89525