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

12676–12700 of 27719

HighFDA (Drugs)·D-0498-2024·2024-05-22
Losartan Potassium and Hydrochlorothiazide Tablets Recalled for Foreign Plastic Contamination
Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets (50 mg/12.5 mg, lot BLK2304A) due to the presence of a plastic-like foreign substance. The recall affects 1,048 bottles distributed nationwide.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1803-2024·2024-05-22
Medtronic Intracoronary Shunts recalled for potential unsealed sterile packaging
Medtronic Intracoronary Shunts may have compromised sterile packaging, potentially allowing contamination. The FDA Class II recall affects 1,410 units distributed worldwide.
Product
Medtronic Intracoronary Shunts: a) ClearView¿ 1.00 mm Intracoronary Shunt, Model Numbers: 31100; b) ClearView¿ 1.25 mm Intracoronary Shunt, Model Numbers: 31125; c) ClearView¿ 2.00 mm Intracoronary Shunt, Model Numbers: 31200
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1805-2024·2024-05-22
Medtronic Venous Cannulae Recalled for Unsealed Sterile Packaging
Medtronic Perfusion Systems is recalling 17,221 units of venous cannulae due to potential for unsealed sterile packaging. The devices were distributed worldwide to healthcare facilities.
Product
Medtronic Venous Cannulae: a) DLP¿ 20 Fr. Malleable Single Stage Venous Cannula, Model Number 68120, b) DLP¿ 24 Fr. Malleable Single Stage Venous Cannula, Model Number 68124, c) DLP¿ 28 Fr. Malleable Single Stage Venous Cannula, Model Number 68128, d) DLP¿ 30 Fr. Malleab
Category
Medical Device
Distribution
0 states
SevereCPSC·24235·2024-05-16
Electrolux Frigidaire and Kenmore Electric Ranges Recalled for Fire and Burn Hazards
Electrolux is recalling about 203,000 Frigidaire and Kenmore smooth-top electric ranges because heating elements can turn on unexpectedly, fail to turn off, or heat incorrectly, posing fire and burn risks. At least 212 incidents have been reported since 2009, including 14 fires and 8 burn injuries.
Product
Frigidaire and Kenmore Smooth-top Freestanding Electric Ranges
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24236·2024-05-16
CHZHVAN Combination Smoke and Carbon Monoxide Detectors Recalled for Failure to Alert
CHZHVAN combination smoke and carbon monoxide detectors can fail to activate and may not alert users to a fire. About 6,800 units sold online via Amazon.com from August 2023 through January 2024 are affected.
Product
CHZHVAN Combination Smoke and Carbon Monoxide Detectors
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24237·2024-05-16
Kano Laboratories Recalls Super Lube Products for Non-Child-Resistant Packaging
Kano Laboratories is recalling Super Lube Syncopen Synthetic Penetrant, Fire Resistant Hydraulic Fluid, and Metal Protectant and Corrosion Inhibitor products in sizes of five gallons or less because the packaging is not child-resistant as required by law, posing a poisoning risk to young children.
Product
Super Lube Syncopen Synthetic Penetrant, Super Lube Fire Resistant Hydraulic Fluid, and Super Lube Metal Protectant and Corrosion Inhibitor (consumer sizes of five gallons or less)
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1231-2024·2024-05-15
Chocolate Ice Cream Cookie Sandwiches Recalled for Undeclared Allergens
Belgian Yummies recalls Chocolate Ice Cream Cookie Sandwiches distributed in Florida due to undeclared allergens: milk, eggs, wheat, peanuts, and tree nuts. Consumers with allergies should not consume this product.
Product
Chocolate Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1776-2024·2024-05-15
Stealth S8 neurosurgical navigation software display error affecting surgical guidance
Medtronic's Stealth S8 surgical navigation software has a display bug that may omit digits, letters, or decimals from critical readings during brain surgery. FDA classified this as Class I due to serious potential surgical errors.
Product
Stealth S8 Clinical Software Application, REF: 9735762, CE0344, Rx Only. Used in the StealthStation System as an aid for locating anatomical structures in either open or percutaneous neurosurgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1224-2024·2024-05-15
D-LO's Pistachio Cheesecake Recalled for Undeclared Allergens and Food Coloring
D-LO's Delightful Gourmet Cheesecake in pistachio flavor is being recalled due to undeclared wheat and soy allergens and undeclared food colors. The product poses a health risk to consumers with allergies to these ingredients.
Product
D-LO's Delightful Gourmet Cheesecake, Pistachio, 142g single serve UPC 8 60007 40398 9, and 678g six serving UPC 8 60007 40395 8, both serving sizes in clear plastic container with hinged lid
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1233-2024·2024-05-15
Belgian Yummies Salted Caramel Ice Cream Cookie Sandwiches recalled for undeclared allergens
Belgian Yummies is recalling Salted Caramel Ice Cream Cookie Sandwiches distributed in Florida due to undeclared allergens including milk, eggs, soy, wheat, peanuts, and tree nuts. The recall affects 254 units.
Product
Salted Caramel Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1733-2024·2024-05-15
Hologic BioZorb Bioabsorbable Markers Recalled for Adverse Events
Hologic is recalling BioZorb Marker bioabsorbable surgical markers due to reported adverse events including infection, pain, device migration, and erosion. FDA classified this as Class I, affecting 53,492 units nationwide.
Product
BioZorb Marker-BioZorb 3D Bioabsorbable Marker-Intended Use radiographic marking of sites in soft tissue. 1) F0405 BioZorb Marker 4cm x 5cm 2) F0404 BioZorb Marker 4cm x 4cm 3) F0331 BioZorb Marker 1cm x 3cm x 3cm 4) F0231 BioZorb Marker 1cm x 3cm x 2cm 5) F0221 BioZorb Mark
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1236-2024·2024-05-15
Belgian Yummies ice cream recalled for undeclared milk and wheat
Belgian Yummies Homemade Ice Cream Horchata Gelato distributed in Florida is recalled due to undeclared milk and wheat allergens that may affect consumers with allergies.
Product
Belgian Yummies Homemade Ice Cream Horchata Gelato. Packaged in 4.75 Liter gray pan.
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1730-2024·2024-05-15
Vyaire Twin Tube Sample Line Nozzle Separation Recall
Vyaire Medical recalls Twin Tube sample line 240 cm devices (Model V-707327) due to potential nozzle separation during patient use. All lots manufactured prior to June 2023 are potentially affected.
Product
Vyaire Medical GmbH, Vyaire Twin Tube sample line 240 cm, Model Number V-707327; The TwinTube sample line 240cm is used in the Vyntus CPX. The TwinTube sample line 240cm is connected to the adapter for DVT. Twin Tube Probenschlauch (707004), which is sold outside the US only.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1232-2024·2024-05-15
Raspberry Ice Cream Cookie Sandwich Recalled for Undeclared Allergens
Belgian Yummies is recalling Raspberry Ice Cream Cookie Sandwiches distributed in Florida due to undeclared allergens including milk, eggs, wheat, peanuts, and tree nuts. Consumers with allergies should not consume these products.
Product
Raspberry Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1609-2024·2024-05-15
Insulin pump app may crash and drain battery, risking insulin delivery interruption
Tandem's t:connect app version 2.7+ may crash repeatedly, draining the insulin pump battery faster than expected and potentially interrupting insulin delivery.
Product
t:connect mobile app used in conjunction with t:slim X2 insulin pump with Control-IQ technology
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1235-2024·2024-05-15
Peanut Butter Ice Cream Cookie Sandwich Recalled: Undeclared Allergens
Belgian Yummies is recalling Peanut Butter Ice Cream Cookie Sandwiches distributed in Florida due to undeclared milk, eggs, wheat, peanuts, and tree nuts. Consumers with allergies should not consume the product.
Product
Peanut Butter Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
Category
Food
Distribution
0 states
SevereFDA (Drugs)·D-0486-2024·2024-05-15
Sapropterin Dihydrochloride Powder for Oral Solution Recalled Due to Sub-Potency
Dr. Reddy's Laboratories is recalling 2,402 cartons of Sapropterin Dihydrochloride Powder 100mg due to sub-potency associated with powder discoloration. The affected lot (T2200352) was distributed nationwide.
Product
Sapropterin Dihydrochloride Powder for Oral Solution 100mg, 30 individual packets per carton, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 43598-477-30.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1230-2024·2024-05-15
Vanilla Ice Cream Cookie Sandwiches Recalled for Undeclared Allergens
Belgian Yummies is recalling Vanilla Ice Cream Cookie Sandwiches distributed in Florida due to undeclared allergens: milk, eggs, wheat, peanuts, and tree nuts.
Product
Vanilla Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
Category
Food
Distribution
0 states
SevereFDA (Drugs)·D-0485-2024·2024-05-15
Prescription Drug Javygtor Recalled for Sub-Potency and Powder Discoloration
Dr. Reddy's Laboratories is recalling Javygtor powder packets nationwide due to powder discoloration and sub-potency. The recall affects 17,332 cartons with multiple lot numbers.
Product
JAVYGTOR — JAVYGTOR (SAPROPTERIN DIHYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1234-2024·2024-05-15
Key Lime Ice Cream Cookie Sandwiches Recalled for Undeclared Allergens
Belgian Yummies is recalling Key Lime Ice Cream Cookie Sandwiches distributed in Florida due to undeclared allergens: milk, eggs, soy, wheat, peanuts, and tree nuts. Consumers with these allergies should not consume the product.
Product
Key Lime Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1768-2024·2024-05-15
Hemodialysis vascular access kit recalled due to metal shavings risk
DURAMAX hemodialysis vascular access kits are recalled due to potential metal shavings that could enter the bloodstream and require surgical removal. Thirty units distributed in Virginia are affected.
Product
DURAMAX STACKED TIP 28CM STR. BASIC KIT, 1-UP PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103028041
Category
Medical Device
Distribution
1 state
HighFDA (Food)·F-1215-2024·2024-05-15
Java Wafer Cookies Recalled for Undeclared Milk Allergen
Sacramento Cookie Factory is recalling Java Wafer - Mocha Hazelnut cookies because they contain undeclared milk, a common allergen that poses a health risk to people with milk allergies.
Product
Java Wafer - Mocha Hazelnut [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]
Category
Food
Distribution
14 states
HighFDA (Food)·F-1216-2024·2024-05-15
Tea Wafers with Vanilla Almond Recalled for Undeclared Milk
Sacramento Cookie Factory recalled Tea Wafers with Vanilla Almond flavor due to undeclared milk allergen. The product was distributed to multiple states and may pose a risk to consumers with milk allergies.
Product
Tea Wafer - Vanilla Almond [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]
Category
Food
Distribution
14 states
HighFDA (Devices)·Z-1763-2024·2024-05-15
Duraflow 2 vascular catheter kit recalled for loose metal shavings
Angiodynamics Inc. is recalling DURAFLOW 2 vascular catheter kits used for hemodialysis and apheresis access due to potential metal shavings that may detach and travel through the vascular system, potentially requiring surgical removal.
Product
DURAFLOW 2, 55CM STRAIGHT BASIC KIT PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012115
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1778-2024·2024-05-15
GE Innova IGS Fluoroscopic X-Ray Systems Adhesive Defect Recall
GE Healthcare is recalling certain Innova IGS x-ray systems due to potential adhesive defects on component bolts. Missing adhesive could cause the detector or x-ray tube to fall during use.
Product
GE Healthcare Innova IGS 6, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

12676–12700 of 27719