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

4401–4425 of 36541

SevereFDA (Drugs)·D-0310-2024·2024-02-14
FDA Recalls Rugby Lubricating Tears Eye Drops for Non-Sterility
Rugby brand Lubricating Tears Eye Drops have been recalled nationwide for non-sterility. Kilitch Healthcare India Limited initiated the voluntary recall of 56,520 bottles due to potential contamination concerns.
Product
Rugby brand Lubricating Tears Eye Drops (Dextran 70 0.1%, Hypromellose 2910 0.3%), packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: Rugby Laboratories, Livonia, MI 48152, NDC 0536-1282-94
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0294-2024·2024-02-14
CVS Health Lubricating Gel Drops Recalled Due to Non-Sterility
CVS Health brand Lubricating Gel Drops are being recalled due to non-sterility concerns. The voluntary recall affects approximately 110,832 bottles distributed nationwide.
Product
CVS Health brand Lubricating Gel Drops (Polyethylene glycol 400 0.4% and Propylene glycol 0.3%), packaged in 0.33 FL OZ (10 mL) bottles, Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895. NDC 76168-712-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0296-2024·2024-02-14
CVS Multi Action Relief Drops Recalled for Non-Sterility
CVS brand Multi Action Relief Drops are being recalled nationwide due to non-sterility, which could allow microbial contamination in the product. The voluntary recall covers all lots of the eye drops.
Product
CVS brand Multi Action Relief Drops (Polyvinyl alcohol 0.5%, Povidone 0.6%, Tetrahydrozoline 0.05%) packaged in 0.5 FL OZ (15mL) bottles, Distributed by CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895. NDC 76168-706-15
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0311-2024·2024-02-14
Up&Up Dry Eye Relief Nationwide Recall for Non-Sterility
Up&Up brand dry eye relief (0.5 FL OZ) distributed by Target nationwide is being recalled due to non-sterility. The FDA Class I recall affects all lots of this ophthalmic drug.
Product
Up&Up brand dry eye relief (Carboxymethylcellulose 0.5%) packaged in 0.5 FL OZ (15 mL) each bottles (Twin Pack), Distributed by: Target Corporation Minneapolis, MN 55403, NDC 76168-800-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0857-2024·2024-02-14
Makana Brownie Boxes Recalled for Undeclared Peanut Allergen
Big Island Candies is recalling Makana Brownie Assortment Boxes distributed in Hawaii due to undeclared peanut allergen and potentially wrong products in some boxes, posing serious risk to consumers with peanut allergies.
Product
Makana Brownie Assortment Box Golden Macadamia Nut Brownie Milk Chocolate Covered Macadamia Nut Brownie Dark Chocolate Covered Macadamia Nut Brownie Made in Hawaii by Big Island Candies, Inc. Hilo Flagship Retail Gift Shop and Factory Big Island of Hawaii Ala Moana Center Street
Category
Food
Distribution
1 state
SevereFDA (Drugs)·D-0301-2024·2024-02-14
FDA recalls Leader brand Lubricant Eye Drops nationwide for non-sterility
Leader brand Lubricant Eye Drops (0.6% Propylene glycol) are recalled nationwide due to non-sterility concerns. Consumers should discontinue use immediately.
Product
Leader brand Lubricant Eye Drops (Propylene glycol Eye Drops 0.6%), packaged in 0.33 FL OZ (10 mL) bottles, Cardinal Health Dublin, Ohio 43017, NDC 70000-0587-1
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0302-2024·2024-02-14
Drug recall: Velocity Pharma Lubricating Eye Drops non-sterility risk
Kilitch Healthcare is recalling all lots of Velocity Pharma Lubricating Eye Drop due to non-sterility issues. The product was distributed nationwide; consumers should stop using it immediately.
Product
Velocity Pharma brand Lubricating Eye Drop (Propylene glycol Eye Drops 0.6%), packaged in 3 bottles of 0.33 FL OZ (10 mL) each, Velocity Pharma, NDC 76168-502-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0306-2024·2024-02-14
Drug: Lubricant Eye Drops Recalled Nationwide Due to Non-Sterility
Kilitch Healthcare India Limited is recalling 7,200 bottles of Lubricant Gel Drops distributed nationwide by Rite Aid due to non-sterility concerns. The manufacturer voluntarily initiated the recall.
Product
Lubricant Gel Drops (Carboxymethylcellulose sodium 1.0%), packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-4540-5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0850-2024·2024-02-14
Cardinal Health Enteral Syringes Recalled for Pump Incompatibility
Cardinal Health Monoject enteral syringes (6, 12, 35, 60 mL) have compatibility issues with certain feeding pumps. The affected lots should not be used with enteral syringe feeding pumps.
Product
Cardinal Health Monoject, 60mL Enteral Syringe (purple) - For Use with ENFit Connection System, REF 460SE
Category
Medical Device
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
SevereFDA (Drugs)·D-0300-2024·2024-02-14
Target Lubricant Eye Drops Recalled for Non-Sterility
Target brand High Performance Lubricant Eye Drops have been recalled nationwide due to non-sterility. The manufacturer, Kilitch Healthcare India Limited, initiated the voluntary FDA Class I recall affecting 401,568 bottles.
Product
Target brand High Performance Lubricant Eye Drops (Polyethylene glycol 400 0.4%, Propylene glycol 0.3%) a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 11673-522-15) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 11673-522-30), Distributed by: Target Corporation Minneapolis, MN
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0847-2024·2024-02-14
Cardinal Health Monoject Enteral Syringes Recalled for Pump Incompatibility
Cardinal Health Monoject enteral syringes (6, 12, 35, 60 mL) in Lot 230503 and 230701 have compatibility issues with certain feeding pumps and should not be used.
Product
Cardinal Health Monoject, 6ML Enteral Syringe (purple) Low Dose (LDT) - For Use with ENFit Connection System, REF 406SE
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0304-2024·2024-02-14
Drug Recall: Non-Sterile Lubricant Eye Drops Distributed Nationwide
Rite Aid is recalling lubricant eye drops due to non-sterility concerns. All lots of the Carboxymethylcellulose Sodium 0.5% product are affected.
Product
LUBRICANT EYE DROPS (Carboxymethylcellulose Sodium 0.5%), packaged 0.5 FL OZ (15mL) bottles (Twin Pack), Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-4811-5
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·24V110000·2024-02-14
Volkswagen and Audi Recall 261,257 Vehicles for Fuel Leak Fire Risk
Volkswagen is recalling 261,257 Audi and Volkswagen vehicles because a fuel tank seal defect may cause fuel to leak, increasing fire risk.
Product
VOLKSWAGEN — VOLKSWAGEN, AUDI GTI, A3, GOLF, GOLF SPORTWAGEN
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0290-2024·2024-02-14
CVS Health Lubricant Eye Drops Recalled Due to Non-Sterility
CVS Health brand Lubricant Eye Drops are being recalled due to non-sterility concerns. Kilitch Healthcare India Limited initiated this voluntary recall affecting 386,256 bottles distributed nationwide.
Product
CVS Health brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%), packaged in a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 76168-702-15) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 76168-702-30), Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 028
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·24E016000·2024-02-14
Aisin Front Passenger Air Bag Sensor Recall for Unintended Deployment
Aisin World Corp. of America is recalling certain front passenger air bag weight sensor assemblies that may crack and short circuit, potentially causing unintended deployment or failure to deploy.
Product
AIR BAGS:SENSOR:OCCUPANT CLASSIFICATION:FRONT PASSENGER recall
Category
Vehicle
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
SevereFDA (Devices)·Z-0853-2024·2024-02-14
Cardinal Health Monoject Syringes Recalled Due to Manufacturing Changes
Cardinal Health is removing all sizes of Monoject sterile syringes and enteral syringes from the market due to manufacturing and rebranding changes. Products were distributed in the US and Canada.
Product
Cardinal Health Monoject, 6 mL Syringe Luer-Lock Tip Soft Pack, REF 1180600777
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0851-2024·2024-02-14
Cardinal Health Monoject Syringes and Enteral Syringes Removed
Cardinal Health is removing all Monoject sterile syringes and enteral syringes due to manufacturing changes and rebranding efforts. These products are distributed across the U.S. and Canada.
Product
Cardinal Health Monoject, 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, REF 1180100777
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0858-2024·2024-02-14
Sandwich Recalled for Undeclared Egg in Authentic Fresh Club
MG Foods Middletown is recalling approximately 852 units of Authentic Fresh to You Deluxe Triple Decker Club sandwiches (8.8oz) because they contain undeclared egg. The products were distributed to PA, NJ, MD, and NY.
Product
Authentic Fresh to You Deluxe Triple Decker Club Net Wt. 8.8oz (254g). Product packaged in a plastic PET container.
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-0929-2024·2024-02-14
BrightView Gamma Camera Detector May Fall and Injure Patients
Philips BrightView gamma camera detectors may fall due to component failure, potentially causing patient injury including lacerations and fractures. The FDA is recalling all affected units.
Product
BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit format 453560279781 453560279791 453560279811 453560279801; 4x4 digit format 2170-3000A 2170-3001A 2170-3002A 2170-3003A
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V107000·2024-02-13
Hyundai Recalls Genesis Models Due to Starter Solenoid Fire Risk
Hyundai is recalling certain 2015-2019 Genesis vehicles because water in the starter solenoid can cause an electrical short and engine fire.
Product
HYUNDAI — HYUNDAI, GENESIS GENESIS, G80, G90, G70
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·006-2024·2024-02-12
Fratelli Beretta Recalls Ready-to-Eat Charcuterie Due to Under Processing
Fratelli Beretta USA is recalling ready-to-eat charcuterie products containing Coppa due to possible under processing and Salmonella contamination.
Product
Fratelli Beretta USA, INC. — Fratelli Beretta USA, Inc. Recalls Ready-To-Eat Charcuterie Meat Products Due to Possible Under Processing
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·24V098000·2024-02-09
Vermeer Recalls BC1800XL Trailers Due to Tongue Weldment Crack Risk
Vermeer is recalling 2016-2024 BC1800XL brush chipper trailers because the tongue weldment may crack and separate from the tow hitch, increasing crash risk.
Product
VERMEER — VERMEER BC1800XL
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24E012000·2024-02-09
Carrier Recalls PowerLINE Generator Sets Due to Overheating Catalyst Fire Risk
Carrier is recalling specific PowerLINE generator sets because the Diesel Oxidation Catalyst may overheat, potentially melting parts and causing a fire.
Product
EQUIPMENT recall
Category
Vehicle
Distribution
Distributed nationwide

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4401–4425 of 36541