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

1226–1250 of 5642

SevereFDA (Devices)·Z-1664-2024·2024-05-22
Expo 5F Selective Angiographic Catheters Recalled for Material Delamination
Boston Scientific is recalling specific batches of Expo 5F Selective Angiographic Catheters due to polyurethane delamination and material detachment that prevents guidewire advancement. The affected catheters may not function properly during angiographic procedures.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO JIG4 (5PK), REF H749085262532; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1659-2024·2024-05-22
Expo selective angiographic cardiac catheters recalled for guidewire advancement failure
Boston Scientific is recalling Expo 5F selective angiographic catheters due to polyurethane layer delamination and material detachment that prevents guidewire advancement through the device.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL5 125CM (5PK), REF H749085262352; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1650-2024·2024-05-22
Expo 5F Selective Angiographic Catheters Recalled for Material Delamination
Boston Scientific is recalling certain batches of Expo 5F Selective Angiographic Catheters due to polyurethane delamination and material detachment in the catheter's inner lining, which prevents proper advancement of the guidewire.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IMT (5PK), REF H749085262022; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Drugs)·D-0494-2024·2024-05-22
Dietary Supplement Marketed as Unapproved Drug Without FDA Approval
Stop Clopez Corp's Schwinnng Herbal Dietary Supplement Capsules were distributed worldwide via Amazon without FDA approval as a new drug. Consumers should discontinue use immediately.
Product
Schwinnng Herbal Dietary Supplement Capsules, packaged in 10-count boxes, distributed by VSD Productions Inc., Las Vegas, NV.
Category
Drug
Distribution
0 states
SevereFDA (Devices)·Z-1662-2024·2024-05-22
Cardiac Catheters Recalled for Material Delamination Risk
Boston Scientific is recalling Expo 5F Selective Angiographic Catheters worldwide due to polyurethane delamination and material detachment that prevents guidewire advancement.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL6 (5PK), REF H74908526252; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1655-2024·2024-05-22
Expo 5F Selective Angiographic Catheters Recalled for Material Delamination
Boston Scientific recalled Expo 5F Selective Angiographic Catheters due to polyurethane layer delamination and material detachment in certain batches, which can prevent guidewire advancement during cardiac procedures.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL4 (5PK), REF H74908526222; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1670-2024·2024-05-22
Expo 5F Cardiac Catheters Recalled for Polyurethane Delamination Risk
Boston Scientific is recalling Expo 5F Selective Angiographic Catheters due to polyurethane layer delamination in the inner lining. The defect prevents guidewire advancement through the catheter, compromising its function during cardiac procedures.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085265002; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1643-2024·2024-05-22
Cardiac catheters recalled due to polyurethane layer delamination defects
Boston Scientific is recalling Expo 5F Selective Angiographic Catheters due to polyurethane layer defects that prevent proper guidewire insertion. Affected devices may experience material detachment in the catheter lining.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR4 MOD (5PK), REF H74908526052; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1680-2024·2024-05-22
Expo 5F Selective Angiographic Catheters Recalled for Material Delamination
Boston Scientific is recalling Expo 5F Selective Angiographic Catheters due to polyurethane layer delamination and material detachment that can prevent guidewire advancement during cardiac procedures.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR1 (5PK), REF H74908526842; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1668-2024·2024-05-22
Boston Scientific Expo 5F Cardiac Catheters Recalled for Delamination Defect
Boston Scientific is recalling Expo 5F Selective Angiographic Catheters due to polyurethane delamination that prevents guidewire advancement during cardiac procedures. The recall affects 86,898 catheters distributed worldwide.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085263012; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1652-2024·2024-05-22
Cardiac Catheters Recalled Due to Delamination and Device Malfunction
Boston Scientific is recalling 8,725 Expo 5F Selective Angiographic Catheters worldwide due to polyurethane layer delamination and material detachment that prevents guidewire advancement.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL3 (5PK)REF H7490852620A2; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1646-2024·2024-05-22
Expo 5F Selective Angiographic Catheters Recalled for Inner Lining Material Failure
Boston Scientific recalls Expo 5F Selective Angiographic Catheters due to polyurethane layer delamination and material detachment in the catheter's inner lining. This prevents guidewire advancement through the catheter.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO KIMNY (5PK), REF H749085261802; cardiac catheter
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
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 (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 (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 (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 (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-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 (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 (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 (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 (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

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1226–1250 of 5642