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 the agency’s own highest classification or reported deaths or serious injuries, 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

4476–4500 of 39749

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
1 state
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
1 state
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
SevereNHTSA·24V335000·2024-05-14
2025 Freightliner Business Class M2 park brake failure recall
Daimler Trucks North America is recalling 2024-2025 Freightliner Business Class M2 vehicles because the park brake valve module may leak, causing park brake failure or unexpected engagement while driving.
Product
FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V336000·2024-05-14
Thomas Built Buses Recalls 2024-2025 SAF-T-Liner C2 Models for Brake Defect
Daimler Trucks North America is recalling 2024-2025 Thomas Built SAF-T-Liner C2 school buses because a seal defect may cause parking brake failure or unexpected engagement.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2 JOULEY, SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V337000·2024-05-14
Tiffin Recalls 2024-2025 Byway Motorhomes Due to Missing Emergency Exit Window
Tiffin Motorhomes is recalling 2024-2025 Byway models because the secondary emergency exit window in the bedroom was not installed, potentially delaying evacuation during an emergency.
Product
TIFFIN — TIFFIN BYWAY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V332000·2024-05-13
ABC Bus Recalls Van Hool CX35 and CX45 Due to Heater Exhaust Risk
ABC Bus is recalling 2023-2024 Van Hool CX35 and CX45 buses because Hydronic L-II heaters may release excessive exhaust gas, posing a risk of smoke poisoning or fire.
Product
VAN HOOL — VAN HOOL CX35, CX45
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V330000·2024-05-10
Lincoln Corsair transmission control software defect causes unexpected neutral shift
Ford is recalling 2021-2022 Lincoln Corsair vehicles due to a hybrid powertrain control module software defect that may cause the transmission to shift into neutral unexpectedly, resulting in loss of drive power and increased crash risk.
Product
FORD — FORD, LINCOLN MAVERICK, ESCAPE, CORSAIR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V329000·2024-05-10
Ford Recalls 2024 F-150 Trucks Due to Steering Column Fastener Defect
Ford is recalling 2024 F-150 vehicles because an incorrect fastener on the steering column may cause loss of steering control, increasing crash risk.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V323000·2024-05-10
Spartan Fire Recalls 2022-2024 Fire Apparatus Due to Seat Fastener Defect
Spartan Fire is recalling 2022-2024 Gladiator, Metro Star, and FC-94 vehicles because undersized seat mount fasteners may break, increasing injury risk in a crash.
Product
SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR, FC-94
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V325000·2024-05-10
Forest River Recalls 2024 Aurora Travel Trailers Due to Wiring Defect
Forest River is recalling 2024 Aurora travel trailers because an incorrectly wired breakaway switch may fail to activate if the trailer detaches, increasing crash risk.
Product
FOREST RIVER — FOREST RIVER AURORA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V322000·2024-05-09
Oliver LEGACY ELITE II Travel Trailers Towing Coupler Defect
Oliver is recalling 1,304 LEGACY ELITE II trailers (2009-2024) due to an underrated towing coupler that may break, creating a risk of trailer detachment and crash.
Product
OLIVER TRAVEL TRAILERS — OLIVER TRAVEL TRAILERS LEGACY ELITE II
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1692-2024·2024-05-08
Left ventricular assist system implant kit recalled for potential inflow cannula seal leak
Thoratec HeartMate 3 left ventricular assist system implant kits may develop a leak at the seal interface between the inflow cannula and titanium apical cuff, potentially compromising device function.
Product
Thoratec HeartMate 3, LVAS Implant Kit, REF:106524US, Sterile EO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1693-2024·2024-05-08
Thoratec HeartMate 3 Left Ventricle Assist System Recalled for Seal Leak
Thoratec recalls HeartMate 3 left ventricle assist systems due to potential leaks at the seal interface. The FDA Class I recall affects 659 implanted devices worldwide.
Product
Thoratec HeartMate 3, LVAS Implant Kit, REF:106524INT, Sterile EO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1238-2024·2024-05-08
King Kullen Broccoli Cutlets Recalled for Undeclared Wheat and Sesame
King Kullen Broccoli Cutlets with Breadcrumbs and Parmesan are being recalled because they contain undeclared wheat and sesame, which can cause allergic reactions in sensitive consumers.
Product
King Kullen Broccoli Cutlets with Breadcrumbs and Parmesan; 20oz; oven safe tin package with a clear dome top marked with a UPC Code 0 8531610145 0
Category
Food
Distribution
1 state
SevereNHTSA·24E037000·2024-05-06
AFCO Legend Revo Arc Remote Reservoir FLH Kits Recall for Suspension Brackets
AFCO Performance Group is recalling Legend Revo Arc Remote Reservoir FLH kits because rear suspension fluid reservoir mounting brackets may crack and break.
Product
SUSPENSION recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V264000·2024-05-06
Autocar Recalls 2020-2024 Legend Vehicles Due to Wiring Fire Risk
Autocar is recalling 2020-2024 Legend vehicles because the wiring harness may route fusible links too closely to other components, increasing the risk of a fire during a short circuit.
Product
AUTOCAR — AUTOCAR LEGEND
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24E035000·2024-05-03
Autoliv Recalls Roof Rail Air Bag Inflators Due to Rupture Risk
Autoliv is recalling specific roof rail air bag inflators that may fail at the weld joint, potentially causing gas leaks or ruptures that increase injury risk.
Product
AIR BAGS:SIDE/WINDOW recall
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·24219·2024-05-02
True Manufacturing Commercial Refrigerators with Secop Compressors Fire Hazard
True Manufacturing is recalling about 29,200 commercial refrigerators equipped with Secop compressors that can overheat and catch fire. The firm has received 14 reports of fires causing property damage, with no injuries reported.
Product
Commercial Refrigerators with Secop Compressors
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0455-2024·2024-05-01
Silverback XXX Power male enhancement product recalled for undeclared sildenafil and tadalafil
Pyramids Wholesale Inc. is recalling Silverback XXX Power male enhancement nationwide due to undeclared sildenafil and/or tadalafil. These prescription drugs were not approved by the FDA before marketing.
Product
SILVERBACK XXX POWER MALE ENHANCEMENT, 2 fl. oz., UPC 8 700470 032762
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1612-2024·2024-05-01
Route 92 Medical 070 Access System Recalled for Distal Tip Separation Risk
Route 92 Medical 070 Access System catheters are recalled for potential distal tip separation during neurovasculature procedures. The defect affects 117 units distributed across 30 US states and New Zealand.
Product
Route 92 Medical, 070 Access System, REF 1004, Rxonly , Sterile EO. Used for introduction of interventional devices into the neurovasculature.
Category
Medical Device
Distribution
30 states
CriticalUSDA FSIS·016-2024·2024-05-01
Cargill Recalls Ground Beef Products Due to Possible E. coli O157:H7 Contamination
Cargill Meat Solutions is recalling approximately 16,243 pounds of raw ground beef products shipped to Walmart nationwide due to possible E. coli O157:H7 contamination.
Product
Cargill Beef — Cargill Meat Solutions Recalls Ground Beef Products Due to Possible E. coli O157:H7 Contamination
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0459-2024·2024-05-01
FDA Recalls Alcoholada Gel Pain Reliever Over Methanol Contamination
Alcoholada Gel pain reliever is being recalled because the ethanol ingredient contains methanol contamination. The FDA classified this as a Class I recall affecting 9,625 bottles distributed nationwide.
Product
Alcoholada Gel, Pain Relieving Gel, 0.5% Lidocaine Hydrochloride, packaged in (a) 8.5 fl oz (251 mL) plastic bottle UPC 0 82252 03120 9 (b) 2.2 fl oz (65 mL) plastic bottle, UPC 0 82252 34030 1 , Manufactured in Aruba by Aruba Aloe Balm Inc., Pitastraat 115, Aruba, Dutch…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0451-2024·2024-05-01
Samurai-X Honey 6800 Recalled for Undeclared Drug Ingredients
Samurai-X Honey 6800, manufactured by Pyramids Wholesale Inc., is recalled for containing undeclared sildenafil and/or tadalafil. The product was distributed nationwide and marketed without FDA drug approval.
Product
Samurai-X Honey 6800, UPC 2 56891 27553 3.
Category
Drug
Distribution
Distributed nationwide

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4476–4500 of 39749