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

9051–9075 of 36629

SevereFDA (Drugs)·D-0897-2021·2021-10-06
ceFAZolin Injectable Drug Bags Recalled for Lack of Sterility Assurance
IntegraDose Compounding Services is recalling ceFAZolin 3 G in 0.9% Sodium Chloride injectable bags due to lack of sterility assurance. The recall affects 589 bags distributed to New Hampshire, Massachusetts, and Minnesota.
Product
ceFAZolin 3 G in 0.9% Sodium Chloride, 115 mL Bag for Injection, Sterile Product, IntegraDose Compounding Services, LLC, 719 Kasota Ave SE, Minneapolis, MN. NDC: 71139-7153-1
Category
Drug
Distribution
3 states
SevereNHTSA·21V779000·2021-10-06
Mercedes-Benz Recalls 2021 Sprinter Vans for Electrical Fire Risk
Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter vans because a cable duct defect may cause an electrical short, increasing the risk of a fire.
Product
MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 2500, SPRINTER 3500, SPRINTER 4500
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0845-2021·2021-10-06
Neutrogena Beach Defense Sunscreen Spray Recalled for Benzene Contamination
Johnson & Johnson Consumer, Inc. is recalling Neutrogena Beach Defense water+sun protection sunscreen spray (SPF 60+) in 8.5 oz aerosol cans due to the presence of benzene contamination.
Product
Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM SPF 60+, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%) NET WT. 8.5 OZ. (240 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 11255
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0008-2022·2021-10-06
Ruzurgi (amifampridine) Tablets Recalled for Microbial Contamination
Jacobus Pharmaceutical Company is recalling Ruzurgi (amifampridine) 10 mg tablets due to microbial contamination. Testing found that certain lots exceeded acceptable limits for aerobic bacteria, yeast, and mold.
Product
Ruzurgi (amifampridine) Tablets 10 mg, packaged in 100-count bottles, Rx only, Manufactured by: Jacobus Pharmaceutical Company, Inc, P.O. Box 5290, Princeton, New Jersey 08540, NDC 49938-110-01.
Category
Drug
Distribution
0 states
SevereFDA (Food)·F-1017-2021·2021-10-06
Velvet Ice Cream Raspberry Fudge Cordial Recalled for Undeclared Allergen
Velvet Ice Cream Company is voluntarily recalling Velvet Ice Cream Raspberry Fudge Cordial because it contains an undeclared allergen that is not listed on the label.
Product
Velvet Ice Cream Raspberry Fudge Cordial 1.75 quarts (56oz) 6 quarts per case
Category
Food
Distribution
5 states
SevereFDA (Food)·F-1028-2021·2021-10-06
Chocolate Flavor Recalled for Undeclared Egg Allergen
Medina Baking and Powder Products, Inc. is recalling Chocolate Flavor (1 QT) distributed domestically because it contains egg that was not declared on the label. Consumers with egg allergies face a serious health risk.
Product
Chocolate Flavor, 1 QT
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-2583-2021·2021-10-06
Ultrasound Gels and Lotions Recalled Due to Bacterial Contamination Risk
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical may contain bacterial contamination. The FDA issued a Class I recall on August 18, 2021.
Product
EcoLotion Transmission Lotion, used in ultrasound procedures. Item/Description: NC70481/Eco Lotion 5 liters, NC70482/Eco Lotion with Aloe 5 liters, NC70482C/Eco Lotion with Aloe 5 liters (4); Myossage Lotion, 1 Gallon, Item: NC31208
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0856-2021·2021-10-06
Morphine Sulfate Injection Recalled Due to Defective Vials
Fresenius Kabi USA LLC is recalling 963,000 vials of Morphine Sulfate Injection because some vials are cracked, which compromises sterility assurance. The affected product was distributed nationwide.
Product
MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2587-2021·2021-10-06
GENOSYL DS vasodilator console recalled for reversed gas lines defect
Vero Biotech recalled 3 GENOSYL DS consoles for a manufacturing defect that reverses gas inlet and outlet lines, causing delivery of toxic nitrogen dioxide instead of therapeutic nitric oxide.
Product
GENOSYL DS (Delivery System) console, for use as a vasodilator.
Category
Medical Device
Distribution
2 states
SevereFDA (Devices)·Z-2499-2021·2021-10-06
DeRoyal Procedure Packs with NORMOFLO Warming Sets Recalled for Aluminum Leaching
DeRoyal procedure packs containing Smiths Medical NORMOFLO warming systems are recalled due to potential aluminum ion leaching into warming fluids. The FDA classified this Class I recall affecting 2880 units distributed in Florida and South Carolina.
Product
DeRoyal Procedure Packs containing Smiths Medical NORMOFLO Irrigation Warming Set
Category
Medical Device
Distribution
2 states
SevereFDA (Drugs)·D-0844-2021·2021-10-06
Neutrogena Beach Defense Sunscreen Spray Recalled for Benzene Contamination
Johnson & Johnson Consumer, Inc. is recalling Neutrogena Beach Defense water+sun protection sunscreen spray (SPF 50) due to the presence of benzene contamination. The recall affects 1,437,804 aerosol cans distributed nationwide.
Product
Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM SPF 50, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%), NET WT. 6.5 OZ. (184 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 11254
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0896-2021·2021-10-06
ceFAZolin Injectable Recalled for Lack of Sterility Assurance
IntegraDose Compounding Services LLC is recalling ceFAZolin 2 G/20 mL sterile syringes for injection due to lack of sterility assurance. Approximately 2,614 syringes distributed in NH, MA, and MN are affected.
Product
ceFAZolin, 2 G/20 mL in Sterile Water, 20 mL Sterile Syringe for Injection, IntegraDose Compounding Services, LLC, 719 Kasota Ave SE, Minneapolis, MN. NDC 71139-7087-1
Category
Drug
Distribution
3 states
SevereNHTSA·21V778000·2021-10-06
Blue Bird Recalls 2022 Vision School Buses Due to Brake Line Defect
Blue Bird is recalling 135 2022 Vision school buses because a missing clamp may cause brake fluid leaks and loss of braking ability.
Product
BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2518-2021·2021-10-06
FDA Recalls Ultrasound Gels for Bacterial Contamination Risk
Omnisound Gel and EcoGel 200 ultrasound gels distributed nationwide from January 2018 to August 2021 may contain bacterial contamination. The FDA issued a Class I recall; health care providers should immediately stop using these products.
Product
Omnisound Gel, 250 ml bottle and 5 L container; and EcoGel 200, 250 ml bottle; Manufactured by Eco-Med. For use in ultrasound procedures.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0899-2021·2021-10-06
Testosterone Cypionate/Propionate Injection Recalled for Sterility Assurance
New Vitalis Pharmacy is recalling Testosterone Cypionate and Testosterone Propionate injections nationwide due to lack of assurance of sterility. The recall affects 1,347 vials distributed across multiple lots.
Product
Testosterone Cypionate Testosterone Propionate, 180mg/mL, 20mg/mL, 1 mL vial, Rx only, New Vitalis Pharmacy 4139 Cadillac Ct # 201 Louisville, KY 40213
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V775000·2021-10-04
Peach Cargo Recalls 2021-2022 Trailers Due to Improperly Tightened Spindle Nuts
Peach Cargo is recalling 2021-2022 Cargo Trailers because improperly tightened spindle nuts may cause axle vibration and overheating, increasing crash risk.
Product
PEACH CARGO — PEACH CARGO CARGO TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V774000·2021-10-04
Nissan Recalls Hybrid SUVs for Software-Related Loss of Drive Power
Nissan is recalling certain 2014-2017 hybrid SUVs because software may shut down the engine, causing a loss of drive power and increasing crash risk.
Product
NISSAN — NISSAN, INFINITI PATHFINDER HYBRID, QX60 HYBRID, MURANO HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21E087000·2021-10-01
Arcimoto Recalls TRiO Conversion Kits Due to Bolt Failure Risk
Arcimoto is recalling TRiO conversion kits because a connecting bolt may fail, causing immediate loss of traction power and increasing crash risk.
Product
EQUIPMENT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V770000·2021-10-01
2021 Ford Bronco Passenger Air Bag Vent Deployment Defect
Ford is recalling certain 2021 Bronco vehicles because the passenger air bag vent may open prematurely during deployment, increasing the risk of injury during a crash.
Product
FORD — FORD BRONCO
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·21V766000·2021-09-30
Volvo Recalls S60 and S80 Vehicles for Air Bag Inflator Defect
Volvo is recalling 2001-2009 S60 and 2001-2006 S80 vehicles because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.
Product
VOLVO — VOLVO S60, S80
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V764000·2021-09-30
Highland Ridge RV Recalls 2021 Open Range Trailers Due to Fire Risk
Highland Ridge RV is recalling 2021 Open Range recreational trailers because the cooktop cabinet may not be sealed from the furnace, creating a fire risk.
Product
HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OPEN RANGE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V762000·2021-09-30
Jayco Recalls 2021-2022 Flight SLX Trailers Due to Fire Risk
Jayco is recalling 2021-2022 Flight SLX travel trailers because the cooktop may not be sealed from the furnace, creating a fire risk.
Product
JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0819-2021·2021-09-29
X Rated Honey For Men Recalled for Undisclosed Tadalafil
Phe Inc is recalling X Rated Honey For Men packets nationwide because the product contains Tadalafil and was marketed without FDA approval. Consumers should stop use immediately.
Product
X RATED HONEY FOR MEN, packaged in 15g packets, 4 packets per box, UPC 6 13682 41232 2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0830-2021·2021-09-29
Avicel RC-591 NF Bulk Powder Recalled for Microbial Contamination
DuPont Nutrition USA is recalling Avicel RC-591 NF bulk powder (lot #2173766940) due to out-of-specification microbial contamination. The product was distributed as a component in finished drug formulations nationwide.
Product
Avicel RC-591 NF (MCC/Carboxymethylcellulose Sodium) NF, bulk powder, 80.0 KG drum, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1009-2021·2021-09-29
Banquet Cut European Style Cold Smoked Salmon Recalled for Botulinum Risk
Seabear Company is recalling Banquet Cut European Style Cold Smoked Salmon due to potential for growth of Clostridium botulinum. The affected product was distributed in Arizona, California, and Georgia.
Product
Banquet Cut European Style Cold Smoked Salmon, Item Number 2-92845, brand Gerard and Dominique Seafoods, packaged in pouch, net wt. per pouch is random, frozen, UPC of pouch: 2 92845 00250 3. The storage/thawing instructions on the pouch is read in parts: "***KEEP FROZEN UNTIL
Category
Food
Distribution
3 states

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9051–9075 of 36629