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

4851–4875 of 39749

SevereFDA (Devices)·Z-0980-2024·2024-02-21
Impella Cardiac Support Catheters: Risk of Left Ventricle Perforation
Impella cardiac catheters are being recalled due to risk of left ventricle perforation during operator use. The FDA has classified this Class I recall affecting 91,914 units worldwide.
Product
Impella catheters - Intravascular micro axial blood pumps that support a patient's circulatory system. (1) Product Code 005042 - Impella 2.5 (2) Product Code 005062 - Impella 5.0 (3) Product Code 005082- Impella LD (7) Product Codes 0550-0008 and 1000100 - Impella 5.5…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0874-2024·2024-02-21
Mighty Fine Chocolate Ice Cream Recalled for Undeclared Peanuts
Byrne Dairy, Inc is recalling Mighty Fine Chocolate Ice Cream because it contains undeclared peanuts. Consumers with peanut allergies should not consume this product.
Product
Mighty Fine Chocolate Ice Cream
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0867-2024·2024-02-21
Al Amir Fresh Foods Hummus Recalled for Undeclared Sesame Allergen
Al Amir Fresh Foods Classic Hummus Creamy Garbanzo is recalled because it contains sesame (tahini) but the label does not declare sesame as an allergen. Consumers with sesame allergies may experience allergic reactions.
Product
Al Amir Fresh Foods Classic Hummus Creamy Garbanzo, packaged in round plastic clear container, net wt. 8oz. There are 12 containers per case. UPC on 8oz container: 7 55134 12341 4. The recalled product label declares: Ingredients: Garbanzo Beans, Tahini Paste, Garlico (Fresh…
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0875-2024·2024-02-21
Fresh Express Chopped Salad Kit Southwest Recalled for Listeria Risk
Fresh Express Incorporated is recalling Chopped Salad Kit Southwest products due to potential Listeria monocytogenes contamination in the cheese condiment pack. Consumers should not consume the product.
Product
Chopped Salad Kit Southwest with condiments(toppings that include cheese), labeled salad bag (Green Cabbage, Green Leaf Lettuce, Kale, Red Cabbage, Carrots, Green Onions, Tortilla Strips, Cheddar Cheese, and Chipotle Ranch Dressing), Net Wt 13.4 oz, 6 bags per case. UPC…
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-0962-2024·2024-02-21
GE Healthcare Lullaby Incubator bedside panels may fail to latch properly
GE Healthcare Lullaby Incubator bedside panels and portholes may appear closed but not be properly latched. If impacted, these panels can disengage and fall open, creating a fall risk for patients.
Product
GE Healthcare Lullaby Incubator Model Hood Door FRU kit, Part Numbers: M1169767, M1160674, M1187512, M1206646, M1166822
Category
Medical Device
Distribution
0 states
SevereNHTSA·24V121000·2024-02-19
Volvo Recalls 2024-2025 VNL and VNR Trucks for Steering Defect
Volvo Trucks is recalling 2024-2025 VNL and VNR models because improperly heat-treated steering gear shafts may crack, risking loss of steering control.
Product
VOLVO — VOLVO VNL, VNR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V120000·2024-02-19
2023–2024 Horton Ford Emergency Vehicles Brake Line Recall
Halcore Group, Inc. is recalling certain 2023–2024 Horton emergency vehicles built on Ford F-450, F-550, and F-600 chassis because the left rear brake line can contact and be damaged by the strut mount when the rear suspension is lowered, risking brake fluid leakage and loss of brakes.
Product
HORTON — HORTON FORD F-450, FORD F-600, FORD F-550
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V119000·2024-02-19
Keystone Recalls 2024 Hideout and Springdale Travel Trailers for Propane Holder Defect
Keystone RV Company is recalling 2024 Hideout and Springdale travel trailers because insufficient welds on the propane cylinder holder may allow the cylinder to detach.
Product
KEYSTONE — KEYSTONE HIDEOUT, SPRINGDALE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V118000·2024-02-16
Mercedes-Benz Recalls 2020-2023 GLE and GLS Models for Transmission Software Defect
Mercedes-Benz is recalling 2020-2023 GLE 450 and GLS 450 vehicles because a transmission software defect may cause the engine to stall, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLS 450, GLE 450, GLS 450 4MATIC, GLS450
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V116000·2024-02-16
Forest River Recalls Sanibel Fifth Wheels Due to Hitch Failure Risk
Forest River is recalling specific 2015-2017 and 2021-2023 Sanibel fifth wheels because the hitch may fail, increasing the risk of a crash.
Product
PRIME TIME — PRIME TIME SANIBEL
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V115000·2024-02-16
Mercedes-Benz Recalls 31,848 Vehicles for Defective 80-Amp Fuses
Mercedes-Benz is recalling 31,848 vehicles because defective 80-Amp fuses may fail, causing loss of drive power, safety functions, or fire.
Product
MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S 580, S 580 E 4MATIC, AMG EQS, S 680
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V117000·2024-02-16
Mercedes-Benz Recalls 2024 GLE Models Due to Accelerator Pedal Bracket Defect
Mercedes-Benz is recalling 2024 GLE 350, GLE 450, and AMG GLE53 vehicles because an improperly welded accelerator pedal bracket may break or detach, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG GLE53 4MATIC+, GLE 350, GLE 450
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·007-2024·2024-02-15
Don Novo & Son Recalls Ready-to-Eat Meat Products Due to Listeria
Don Novo & Son is recalling approximately 9,330 pounds of ready-to-eat meat products in Florida due to possible Listeria monocytogenes contamination.
Product
Don Novo & Son — Don Novo & Son Recalls Ready-To-Eat Meat Products Due to Possible Listeria Contamination
Category
Food
Distribution
1 state
CriticalFDA (Devices)·Z-0857-2024·2024-02-14
Cardinal Health Monoject Syringes Recalled Due to Manufacturing Changes
Cardinal Health is recalling all sizes of Monoject sterile syringes—including Luer-Lock and Enteral syringes with ENFit connections—due to manufacturing and rebranding changes. Products distributed across the U.S. and Canada.
Product
Cardinal Health Monoject, 60 mL Syringe Luer-Lock Tip Soft Pack, REF 1186000777T
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0303-2024·2024-02-14
FDA recalls non-sterile EQUATE lubricant eye drops nationwide
Walmart's EQUATE brand Hydration PF Lubricant Eye Drops are being recalled due to non-sterility. This FDA Class I recall affects 33,984 bottles distributed nationwide.
Product
EQUATE brand Hydration PF Lubricant Eye Drops (Polyethylene glycol 400 0.4% and Propylene glycol 0.3%) packaged in 0.34 FL OZ (10 mL) bottles, Distributed by: Walmart Inc., Bentonville, AR 72712, NDC 79903-168-01
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0855-2024·2024-02-14
Cardinal Health Monoject Syringe and Enteral Syringe Removal Due to Manufacturing Changes
Cardinal Health is removing Monoject sterile syringes (Luer-Lock and Enteral with ENFit) from the market due to manufacturing and rebranding changes. Distribution affected US and Canada.
Product
Cardinal Health Monoject, 20 mL Syringe Luer-Lock Tip Soft Pack, REF 1182000777
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0298-2024·2024-02-14
Drug: CVS Health Lubricant Gel Drops recalled nationwide for non-sterility
CVS Health Lubricant Gel Drops (Carboxymethylcellulose Sodium 1%) are being recalled nationwide due to non-sterility concerns. All lots of the product in single and twin pack bottles are affected.
Product
CVS Health brand, Lubricant Gel Drops (Carboxymethylcellulose Sodium 1%) packaged in a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 76168-704-15) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 76168-704-30), Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI…
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0308-2024·2024-02-14
FDA Class I Drug Recall: Non-Sterile Multi-Action Relief Drops
Rite Aid is recalling Multi-Action Relief Drops nationwide due to non-sterility concerns. The FDA classified this as a Class I recall affecting 9,216 bottles.
Product
Multi-action Relief Drops (Polyvinyl alcohol 0.5%, Providone 0.6%, Tetrahydrozoline Hydrochloride 0.05%), packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-2254-3
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0293-2024·2024-02-14
FDA recalls Rugby brand lubricating eye drops nationwide for non-sterility
Rugby brand Polyvinyl Alcohol 1.4% Lubricating Eye Drops are being recalled nationwide due to non-sterility. The recall affects all lots of the 0.5 FL OZ bottles distributed.
Product
Rugby brand Polyvinyl Alcohol 1.4% Lubricating Eye Drops, packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: Rugby Laboratories, Livonia, MI 48152, NDC 0536-1325-94
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0299-2024·2024-02-14
Drug recall: DRY EYE RELIEF eye drops for non-sterility
FDA recalls DRY EYE RELIEF eye drops nationwide due to non-sterility. The ophthalmic product distributed in 23,208 bottles affects all lots. Consumers should discontinue use immediately.
Product
DRY EYE RELIEF — DRY EYE RELIEF (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0305-2024·2024-02-14
FDA Recalls CVS Health Lubricating Eye Drops Due to Non-Sterility
CVS Health brand Lubricating Eye Drops are being recalled due to non-sterility. The FDA Class I recall affects 45,408 bottles distributed nationwide.
Product
CVS Health brand Mild Moderate Lubricating Eye Drops (Propylene glycol 400 0.25%), packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895. NDC 76168-711-15
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0291-2024·2024-02-14
FDA Recalls Non-Sterile Lubricant Eye Drops Due to Contamination Risk
The FDA recalled approximately 210,192 bottles of Leader brand Lubricant Eye Drops due to non-sterility that could allow contamination. All lots distributed nationwide are affected.
Product
LUBRICANT DROPS — LUBRICANT DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·24V109000·2024-02-14
2023 Triumph Tiger Sport and Trident 660 Front Fork Caps May Detach
Front fork caps on 2023 Triumph Tiger Sport 660 and Trident 660 motorcycles may detach due to incorrectly machined threads, potentially causing loss of vehicle control and crash risk.
Product
TRIUMPH — TRIUMPH redundant TRIDENT 660, TIGER SPORT 660
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0309-2024·2024-02-14
Lubricant Eye Drops Recalled Due to Non-Sterility Concerns
Rite Aid is recalling 7,296 bottles of lubricant eye drops nationwide due to non-sterility. The FDA has classified this as a Class I recall.
Product
Lubricant Eye Drops (Propylene glycol 0.6%), packaged in 0.33 FL OZ (10 mL) each bottle (Twin Pack), Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-4811-3 Retail Labeler: Rite Aid
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0930-2024·2024-02-14
BrightView X Gamma Camera Detector May Fall, Causing Patient Injury
Detectors in Philips BrightView X gamma cameras may fall unexpectedly due to component failure, risking patient injury including fractures and lacerations.
Product
BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478; 12-digit format 453560824741 453560829261;
Category
Medical Device
Distribution
Distributed nationwide

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4851–4875 of 39749