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

9251–9275 of 113902

SevereFDA (Devices)·Z-1698-2025·2025-05-21
AirLife Infant Heated Wire Circuit Adapter Disconnection Risk Recall
Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (model AH265) because adapters may disconnect during setup or use, potentially interrupting ventilation to newborns. Disconnection can cause hypoxia, hypercapnia, and organ failure.
Product
Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH265 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit Kit Dual-limb, Dual-heat, high-flow circuit (>4 L/min) Contains AH165 Circuit, AH290 Chamber Compone
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1697-2025·2025-05-21
AirLife Infant Heated Wire Circuit Adapter Disconnection Risk
Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (Model AH165) because adapters may disconnect during setup or use, interrupting ventilation to infants and potentially causing severe complications.
Product
Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH165 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit dual-limb, dual-heat, high-flow circuit (>4 L/min) Component: No. a conduit for respiratory gas bet
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1727-2025·2025-05-21
iGo2 DC Car Adapter Recall: Overheating and Housing Deformation Risk
Medical Depot Inc. is recalling 89,532 units of the iGo2 DC Car Adapter used with iGo2 Portable Oxygen Concentrator Systems. The DC power supply housing may become excessively hot to the touch and deform, posing a burn and fire hazard.
Product
iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0763-2025·2025-05-21
Bonya Strawberry Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Strawberry Yogurt Parfait cups (8 oz) distributed to NY, PA, MA, and NJ because they contain undeclared almonds, a common allergen.
Product
Bonya Strawberry 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
SevereFDA (Food)·F-0772-2025·2025-05-21
Bonya Passion Fruit Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Passion Fruit Yogurt Parfait (8 oz) due to undeclared almonds, which poses a risk to consumers with tree nut allergies. The product was distributed to New York, Pennsylvania, Massachusetts, and New Jersey.
Product
Bonya Passion Fruit 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
SevereFDA (Food)·F-0770-2025·2025-05-21
Bonya Pineapple Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Pineapple Yogurt Parfait (8oz cups) distributed to NY, PA, MA, and NJ because the product contains undeclared almonds, a common allergen that is not listed on the label.
Product
Bonya Pineapple 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
SevereFDA (Food)·F-0768-2025·2025-05-21
Bonya Lemon Yogurt Parfait Recalled for Undeclared Almonds
Knockroe Inc is recalling Bonya Lemon Yogurt Parfait (8oz) because it contains undeclared almonds, a common allergen. The product was distributed to New York, Pennsylvania, Massachusetts, and New Jersey.
Product
Bonya Lemon 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
SevereFDA (Devices)·Z-1730-2025·2025-05-21
MedicaLyte Liquid Bicarbonate Concentrate Recalled for Foreign Matter
Nipro Renal Solutions USA is recalling MedicaLyte Liquid Bicarbonate Concentrate (models BC+201 and BC+100) due to the potential presence of visible foreign matter in the product.
Product
MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+100 36.83X. Plastic bottle packaged in corrugated shipper cases (4 bottles per shipper case).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0776-2025·2025-05-21
Tomatoes Recall Due to Potential Salmonella Contamination
Ray & Mascari, Inc. is recalling tomatoes sold in retail 4-count clam shell containers and bulk cardboard cases due to potential Salmonella contamination. Affected products were distributed in IN, KY, MA, MD, MI, NC, OH, PA, and WI.
Product
Tomatoes, retail 4 Count Vine Ripe Tomatoes packaged in clam shell containers [20 oz. (1 lb. 4 oz) 567g] with UPC# 7 96553 20062 1; 12 retail clam shells per case. Bulk 25# 6x6 tomatoes (cardboard case), bulk 10# 6x6 Tomatoes (cardboard case), bulk 25# Random #2 Tomatoes (cardbo
Category
Food
Distribution
9 states
SevereFDA (Food)·F-0774-2025·2025-05-21
Bonya Black Cherry Yogurt Parfait Recalled for Undeclared Almonds
Knockroe Inc is recalling Bonya Black Cherry Yogurt Parfait due to undeclared almonds, which pose a risk to people with tree nut allergies. The product was distributed in NY, PA, MA, and NJ.
Product
Bonya Black Cherry 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
SevereFDA (Devices)·Z-1726-2025·2025-05-21
Welch Allyn Life2000 Compressor recalled for cybersecurity vulnerability
Baxter Healthcare Corporation is recalling Welch Allyn Life2000 Compressor units due to a cybersecurity vulnerability discovered during internal testing.
Product
Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1763-2025·2025-05-21
LifeShield Infusion Safety Software Recalled for Drug Library Defects
ICU Medical is recalling LifeShield Drug Library Management software v2.1 and v2.2 due to defects that could allow over-delivery of medication to patients or unauthorized modification of drug parameters.
Product
LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1752-2025·2025-05-21
Pruitt Irrigation Occlusion Catheter Recalled for Incomplete Sterile Seals
LeMaitre Vascular is recalling Pruitt Irrigation Occlusion Catheters (Catalog Numbers 2102-09, E2102-09) due to incomplete sterile barrier seals found during internal testing. The defect affects approximately 26,872 units distributed nationwide and internationally.
Product
Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0809-2025·2025-05-21
Dixit Foods Pohe Recalled for Undeclared Milk and Peanut Allergens
Dixit Foods Pohe (110 g packages) is recalled due to undeclared milk and/or peanut allergens. The product was distributed in California, Utah, and Washington.
Product
Dixit Foods, Pohe, Net Wt. 110 g, Ingredients: Rice Flakes, Groundnuts, Edible Sunflower oil, Sugar, Salt, Green Chilli, Asafoetida, Curry Leaves, Mustard seeds, Turmeric Powder etc, Allergen Information: May contain Peanuts, Treenuts, Wheat, Sesame, Mustard
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1748-2025·2025-05-21
Abbott Alinity m Resp-4-Plex Amplification Kit Recall
Abbott Molecular is recalling the Alinity m Resp-4-Plex Amplification Kit due to reports of reactive negative controls and false positive results in respiratory virus testing.
Product
Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended for the qualitative detection and differentiation of RNA from influenza A virus (flu A), influenza B virus (fl
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0766-2025·2025-05-21
Bonya Mango Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Mango Yogurt Parfait (8oz) because it contains undeclared almonds, a major food allergen. The product was distributed to NY, PA, MA, and NJ.
Product
Bonya Mango 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-1768-2025·2025-05-21
KliniTray surgical alignment system recalled for microbial contamination risk
Klinika Medical is recalling the KliniTray tissue resection margin examination board (Model 2001105-F) due to potential microbial contamination. The device was distributed nationwide in Massachusetts.
Product
KliniTray. KlinioTray. Tissue resection margin examination board/small. Model Number: 2001105-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact orientation and posi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1766-2025·2025-05-21
Centurion Sterile Weitlaner Retractor recalled for sterile packaging puncture risk
Medline Industries is recalling Centurion Sterile Weitlaner Retractor 3 x 4 Prong units because the retractors may puncture through the sterile packaging. The product is distributed nationwide.
Product
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0808-2025·2025-05-21
Dixit Foods Sabudana Khichadi Recalled for Undeclared Milk and Peanut Allergens
Dixit Foods Sabudana Khichadi (200 g) is recalled due to undeclared milk and/or peanut allergens. The product may pose a serious risk to consumers with allergies to these ingredients.
Product
Dixit Foods, Sabudana Khichadi, Net Wt. 200 g, Ingredients: Sago (Sabudana), Crushed Groundnuts, Sugar, DesiGhee, Salt, Green Chilli, Cumin Seeds. Allergen Information: May contain Peanuts, Treenuts, Wheat, Sesame, Mustard
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1762-2025·2025-05-21
Tornado Embolization Microcoil recalled for incorrectly sized coils
Cook Incorporated is recalling Tornado Embolization Microcoils due to incorrectly sized coils in affected lots. The devices are used for vascular embolization procedures.
Product
Tornado Embolization Microcoil, intended for embolization of selective vessel supply to arteriovenous malformations and other vascular lesions, RPN MWCE-18S-3/2-TORNADO (GPN G08261), RPN MWCE-18S-3/2-TORNADO-081800 (GPN G13102), RPN MWCE-18S-4/2-TORNADO (GPN G08357)
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1774-2025·2025-05-21
Philips Intera 1.5T MRI Quadrature Body Coil seal adhesive failure
Philips is recalling Intera 1.5T MRI systems due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and contact patient skin during scanning.
Product
Intera 1.5T, Model Numbers: 781195 and 781295;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1751-2025·2025-05-21
Pruitt Occlusion Catheter Recalled Due to Incomplete Sterile Barrier Seals
LeMaitre Vascular is recalling Pruitt Occlusion Catheters (catalog numbers 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56) because some packages have incomplete sterile barrier seals, potentially compromising product sterility.
Product
Pruitt Occlusion Catheter. Catalog Numbers: 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56
Category
Medical Device
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-1775-2025·2025-05-21
Philips Intera 1.5T MRI Scanner Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.5T Explorer/Nova Dual MRI scanners (Model 781108) due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges that could contact patients during scanning and cause skin injuries.
Product
Intera 1.5T Explorer/Nova Dual, Model Number: 781108;
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

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9251–9275 of 113902