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

1251–1275 of 5642

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-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
SevereNHTSA·24V832000·2024-05-11
2024 Tesla Cybertruck drive inverter fault may cause power loss
Tesla is recalling 2024 Cybertruck vehicles due to a drive inverter fault that may cause loss of propulsion. Affected owners will receive a free inverter replacement.
Product
TESLA — 2024 TESLA CYBERTRUCK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V836000·2024-05-11
2024-2025 Lucid Air vehicles recalled for wiring harness defect
Lucid is recalling 2024-2025 Air models due to a rear subframe wiring harness that may be too short, causing power loss to the rear drive unit and increasing crash risk. Replacement is free.
Product
LUCID — 2025 LUCID AIR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V697000·2024-05-10
Proterra Transit Buses Recalled for Inverter Power Loss Risk
Proterra is recalling 2019-2022 ZX5 and Catalyst 800V transit buses due to inverter transistor overheating risk. A transistor failure can cause loss of power steering and drive power, increasing crash risk.
Product
PROTERRA — 2021 PROTERRA ZX5
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V653000·2024-05-09
RAM 1500 Models Recalled for Anti-Lock Brake Software Malfunction
Chrysler is recalling certain 2019, 2021-2024 RAM 1500 vehicles because a software malfunction in the ABS control module may disable the electronic stability control system, increasing crash risk.
Product
RAM — 2024 RAM 1500
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
SevereNHTSA·23V588000·2024-05-08
2023 Honda Accord and CR-V Hybrid transmission defect can cause power loss
Honda is recalling certain 2023 Accord Hybrid and CR-V Hybrid vehicles because the electronic continuously variable transmission (e-CVT) may have been improperly manufactured, potentially resulting in loss of drive power and increased crash risk.
Product
HONDA — 2023 HONDA ACCORD HYBRID
Category
Vehicle
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
0 states
SevereNHTSA·24V412000·2024-05-06
2024 Hyundai Tucson and Santa Cruz power steering defect recall
Hyundai is recalling 2024 Tucson and Santa Cruz vehicles due to a potential circuit board short in the power steering system. Loss of steering assist could increase crash risk.
Product
HYUNDAI — 2024 HYUNDAI TUCSON
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V408000·2024-05-06
Rivian R1S and R1T damaged pillar clips affect airbag deployment
Rivian is recalling certain 2022-2024 R1S and R1T vehicles. Damaged attachment clips on pillar trim panels may prevent proper side curtain airbag deployment in a crash, increasing injury risk.
Product
RIVIAN — 2023 RIVIAN R1S
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V407000·2024-05-06
2023 Kia Telluride power seat motor fire risk recall
Kia is recalling certain 2023 Telluride vehicles due to a fire risk in the front power seat motor caused by a stuck seat slide knob. Owners should park outside until repairs are completed.
Product
KIA — 2023 KIA TELLURIDE
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
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 Caribbe
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1464-2024·2024-05-01
VITEK 2 AST Test Kits: Ceftriaxone Concentration Error Risk
Biomerieux Inc is recalling VITEK 2 AST test kits due to ceftriaxone concentration errors that could produce false susceptible results in antimicrobial susceptibility testing.
Product
VITEK 2 - AST Test kits (in vitro diagnostic test cards for antimicrobial susceptibility): a) AST-N334, REF 418984; b) AST-GN95, REF 421982; c) AST-GN99, REF 423102; d) AST-N390, REF 423340; e) AST-N391, REF 423341; f) AST-N392, REF 423342; g) AST-N395, REF 423491;
Category
Medical Device
Distribution
0 states
SevereFDA (Drugs)·D-0453-2024·2024-05-01
Male Sexual Enhancement Product Recalled for Undeclared Pharmaceutical Ingredients
Pyramids Wholesale Inc. is recalling all lots of GoHARD 25000 because it contains undeclared sildenafil and tadalafil. The product was marketed without FDA approval for these prescription-strength drugs.
Product
GoHARD 25000, Male Sexual Enhancement, Honey, 100% Natural, UPC: N/A.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1204-2024·2024-05-01
Roly Poly Bakery Multigrain Bread Recalled for Undeclared Egg
Roly Poly Bakery is recalling multigrain bread sold in Connecticut and Massachusetts because it contains undeclared egg, a major food allergen. Consumers with egg allergies should not consume this product.
Product
Roly Poly Bakery brand MULTIGRAIN bread; INGREDIENTS: Whole Wheat Flour, High Gluten Flour, Ryechops, Sesame, Caraway, Brownflex, Soybean, Pearl Wheat, Sunflower, Salt, Water.
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-1613-2024·2024-05-01
Route 92 Medical delivery catheter recalled due to tip separation risk
Route 92 Medical is recalling Tenzing 7 delivery catheters because the distal tip may separate from the proximal marker band. The affected units were distributed across the US and New Zealand.
Product
Route 92 Medical, Tenzing 7 Delivery Catheter, REF 1005, Rx Only, Sterile EO. Used for introduction of interventional devices into the neurovasculature.
Category
Medical Device
Distribution
30 states
SevereFDA (Drugs)·D-0456-2024·2024-05-01
The GOAT Sublingual Strip Recalled for Undeclared Prescription Drug Ingredients
The GOAT Sublingual Strip male enhancement product, distributed nationwide, was recalled for containing undeclared sildenafil and tadalafil. The product was marketed without FDA approval.
Product
The GOAT SUBLINGUAL STRIP, MALE ENHANCEMENT, 2 Pack, Distributed by Hombres LLC, 130 Maccormick Ave, Suite 105, Costa Mesa, A, UPC 6 61631 26363 1.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0454-2024·2024-05-01
FDA Recalls libigrow RED DRAGON+ Capsules for Undeclared Sildenafil and Tadalafil
Pyramids Wholesale Inc. is recalling libigrow RED DRAGON+ capsules nationwide because they contain undeclared sildenafil and tadalafil, prescription medications not approved by the FDA for this product.
Product
libigrow RED DRAGON+, Maximum Strength Formula, 2 capsules per box, UPC 7 05105 83073 5.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0457-2024·2024-05-01
Male Performance Enhancer Recalled for Undeclared Sildenafil and Tadalafil
ALPHASTRIP Male Performance Enhancer strips are being recalled nationwide because they contain undeclared sildenafil and tadalafil. The product was marketed without FDA approval.
Product
ALPHASTRIP MALE PERFORMANCE ENHANCER, The fastest acting sublingual, Serving Size (1 strip), Distributed by: GALT INT'L
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1611-2024·2024-05-01
Route 92 Medical Reperfusion System Potential Catheter Tip Separation
Route 92 Medical recalls its Full Length 070 Reperfusion System due to potential distal tip separation at the proximal marker band, which could affect device delivery during interventional procedures.
Product
Route 92 Medical, Full Length 070 Reperfusion System, REF: 7001, Rxonly, SterileEO. Used for Introduction of interventional devices into the neurovasculature.
Category
Medical Device
Distribution
30 states

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