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

8751–8775 of 36629

SevereFDA (Drugs)·D-0236-2022·2021-11-24
LOTRIMIN AF Miconazole Nitrate Powder Spray Recalled for Benzene Contamination
Bayer is recalling LOTRIMIN AF Deodorant Powder Spray due to potential benzene contamination from manufacturing deviations at a facility where other lots were found contaminated. The recall affects 2,817,468 cans distributed nationwide in the US, Puerto Rico, Canada, and Mexico.
Product
LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-1272-2 UPC 3 11017 41023 3
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0224-2022·2021-11-24
FDA Recalls Scrip Ultrasound Gel for Potential Bacterial Contamination
Scrip Inc is recalling Scrip Ultrasound Gel Clear (5L) nationwide due to potential bacterial contamination. Affected units may cause harm if contaminated product contacts patients during ultrasound procedures.
Product
Scrip Ultrasound Gel Clear, 5L Intended for use in acoustic coupling of ultrasound transducer to tissue
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0176-2022·2021-11-24
Greenhead Lobster Frozen Cooked Meat Recalled for Listeria Contamination
Greenhead Lobster brand frozen cooked lobster meat products may be contaminated with Listeria monocytogenes. The recall affects multiple lobster meat products sold in six states.
Product
Greenhead Lobster brand Frozen Cooked Claw and Knuckle Meat - 2lbs; Greenhead Lobster brand Frozen Cooked Claw and Knuckle Meat - 1lb; Greenhead Lobster brand Frozen Cooked Broken Meat - 2lbs; Greenhead Lobster brand Frozen Cooked Tail Meat - 2lbs; Greenhead Lobster brand Fro
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0177-2022·2021-11-24
Pier-C Produce White Onions Recalled for Salmonella Contamination
Pier-C Produce, Inc. is recalling white onions that may be contaminated with Salmonella. The recalled onions were distributed in Florida. Consumers should not eat the affected product.
Product
Pier-C Produce, Inc., White Onions Grade No 1, Net Wt 2 lbs (0.907 KG), Distributed by Pier C Produce, Leamington, Ontario, Produce of Mexico
Category
Food
Distribution
1 state
SevereFDA (Drugs)·D-0238-2022·2021-11-24
LOTRIMIN AF Powder Spray Recalled for Benzene Contamination Risk
Bayer Healthcare is recalling LOTRIMIN AF (Miconazole nitrate 2%) Powder Spray because it was manufactured at a facility where other lots were found contaminated with benzene. The recall affects multiple lot numbers distributed nationwide in the US, Puerto Rico, Canada, and Mexico.
Product
LOTRIMIN AF (Miconazole nitrate 2%) Powder Spray NET WT 133g (4.6 OZ) can, packaged as (a) a single pack NDC 11523-0544-2 UPC 3 11017 41025 7; (b) 3 pack, NDC 11523-0544-2, UPC 0 41100 58594 3; Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, ,
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0234-2022·2021-11-24
Arrow-Trerotola Percutaneous Thrombolytic Device: Inner Lumen Detachment Risk
Arrow International is recalling 1918 units of the Arrow-Trerotola Percutaneous Thrombolytic Device due to inner lumen detachment that can cause embolization, requiring emergency retrieval and delaying treatment.
Product
Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-65709-WC The Arrow-Trerotola" Percutaneous Thrombolytic Device (PTDTM) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0225-2022·2021-11-24
Scrip Creme ultrasound lotion recalled for bacterial contamination
Scrip Creme All Purpose Lotion is being recalled due to bacterial contamination in this ultrasound coupling lotion. The product—1001 gallons in lots distributed between August 2018 and August 2021—was distributed nationwide.
Product
Scrip Creme All Purpose Lotion Intended for use in acoustic coupling of ultrasound transducer to tissue
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0246-2022·2021-11-24
Lotrimin AF Deodorant Powder Spray Recalled for Benzene Contamination
Bayer Healthcare is recalling Lotrimin AF Deodorant Powder Spray (Miconazole nitrate 2%) nationwide due to the presence of benzene contamination. The recall affects approximately 2.8 million cans distributed across the US, Puerto Rico, Canada, and Mexico.
Product
LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray, NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-1272-2 UPC 3 11017 41023 3
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0244-2022·2021-11-24
Tinactin Jock Itch Powder Spray Recall Due to Benzene Contamination
Bayer Healthcare is recalling 592,416 cans of Tinactin (Tolnaftate 1%) Jock Itch Powder Spray distributed nationwide due to potential benzene contamination. The product was manufactured at a facility where other lots were found to be contaminated with benzene.
Product
Tinactin (Tolnaftate 1%) JOCK ITCH POWDER SPRAY NET WT133g (4.6 oz) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Ireland 86951967, UPC 3 11017 41007 3, NDC 11523-0072-5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0174-2022·2021-11-24
White Onions Recalled for Potential Salmonella Contamination
Sysco Merchandising and Supply is recalling white onions packed in 10-pound bags due to potential Salmonella contamination. The affected product was distributed across 15 states.
Product
White onions packed in 10 pound bag
Category
Food
Distribution
15 states
SevereFDA (Food)·F-0206-2022·2021-11-24
EveryPlate Meal Kits Recalled for Salmonella-Contaminated Onions
EveryPlate meal kits distributed nationwide are being recalled because they contain onions purchased from ProSource that are associated with a Salmonella Oranienburg outbreak.
Product
EveryPlate Meal Kit Product Codes 82-83-89-93-94-96-98 from Production Week 36 (production week start date: 09/01/2021)
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0181-2022·2021-11-24
Raw Onions Recalled Due to Potential Salmonella Contamination
Bix Produce Company LLC is recalling raw onions in multiple varieties and package sizes due to potential Salmonella contamination. The recall affects products distributed in Iowa, Minnesota, North Dakota, South Dakota, and Wisconsin.
Product
Raw onion sold in bags or sliced and diced with the following item numbers and lot code. 1. RED JUMBO 25# 1/25 LB, item 06370; 2. ONIONS,RED JUMBO 1/5 LB, item 06373; 3. ONIONS,RED MEDIUM 1/25 LB, item 06380; 4. ONIONS,WHITE JUMBO 50# 1/50 LB, it
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0209-2022·2021-11-24
Kroger Garden Salad Recalled Due to Listeria Contamination
Kroger Garden Salad has been recalled because the Georgia Department of Agriculture detected Listeria monocytogenes in the product. The recall affects specific lot codes distributed to multiple states.
Product
Kroger Garden Salad; iceberg lettuce, shredded carrots, red cabbage; Net Wt. 12 oz. (340g) UPC: 0-11110-91036-3 Distributed by The Kroger Company, Cincinnati, OH
Category
Food
Distribution
10 states
SevereFDA (Food)·F-0171-2022·2021-11-24
Whole White Onions Recalled for Potential Salmonella Contamination
Keeler Family Farms is recalling whole white onions imported from Chihuahua, Mexico due to potential contamination with Salmonella Oranienburg. The affected onions were shipped between July 1 and August 25, 2021.
Product
Whole raw onions - WHITE - imported from Chihuahua, Mexico and shipped from July 1, 2021 through August 25, 2021. Products are packaged in 25 lb. and 50 lb. mesh bags. One pallet contains 42 bags. Store in cool dry place off the ground. Labeling will state product of Mexico on bi
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0199-2022·2021-11-24
EveryPlate Meal Kits Recalled for Salmonella Contamination
EveryPlate meal kits with product codes 83, 84, 86, 89, 92, 94, and 97 from production week July 14, 2021, are recalled due to onions contaminated with Salmonella Oranienburg. The affected onions were purchased from ProSource.
Product
EveryPlate Meal Kit Product Codes 83-84-86-89-92-94-97 from Production Week 29 (production week start date: 07/14/2021)
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0200-2022·2021-11-24
EveryPlate Meal Kits Recalled for Salmonella Contamination
HelloFresh US is recalling specific EveryPlate meal kits containing onions contaminated with Salmonella Oranienburg. The affected products are from production week starting July 21, 2021, with product codes 84, 88, 89, 90, 91, 92, 94, 98, 99, and 100.
Product
EveryPlate Meal Kit Product Codes 84-88-89-90-91-92-94-98-99-100 from Production Week 30 (production week start date: 07/21/2021)
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0184-2022·2021-11-24
Green Giant Fresh Whole White Onions Recalled for Salmonella
Green Giant Fresh brand whole white onions in 2 lb. bags are being recalled due to potential Salmonella Oranienburg contamination. The affected onions were distributed in Minnesota and North Dakota.
Product
Green Giant Fresh brand, Whole WHITE Onions packaged in 2 lb. flexible mesh bags, UPC 60580600218-2.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0207-2022·2021-11-24
Dole Garden Salad Recalled for Listeria monocytogenes
Dole Garden Salad (24 oz) has been recalled because Listeria monocytogenes was detected during testing by the Georgia Department of Agriculture. The affected lots were distributed across ten US states.
Product
Dole Garden Salad; iceberg lettuce, shredded carrots, red cabbage; Net Wt. 24 oz. (1 lb. 8 oz.) 680 g UPC: 0 71430 01136 2 Dole Food Company, Inc. Distributed by Dole Fresh Vegetables, Monterey, CA
Category
Food
Distribution
10 states
SevereFDA (Food)·F-0188-2022·2021-11-24
Fisherman's Wharf Cooked Shrimp Recalled for Listeria Risk
Fisherman's Wharf Shrimp 16/20 Cooked Shrimp 16oz packages are being recalled due to potential contamination with Listeria monocytogenes. The affected products were distributed domestically with specific serial numbers and best-by dates in early April 2023.
Product
Fisherman's Wharf, Shrimp 16 /20 Cooked Shrimp 16oz 7306067
Category
Food
Distribution
0 states
SevereFDA (Drugs)·D-0253-2022·2021-11-24
Tinactin Tolnaftate Powder Spray Recalled Due to Benzene Contamination
Bayer Healthcare Pharmaceuticals is recalling Tinactin (Tolnaftate 1%) Powder Spray because some cans contain benzene contamination. Consumers should stop using affected lots and consult a healthcare provider.
Product
Tinactin (Tolnaftate 1%) POWDER SPRAY NET WT 133g (4.6 oz) can, labeled as (a) Product of Ireland 86940418; (b)Product of Finland 20006106; Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 3 11017 41009 7, NDC 11523-0777-2.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0251-2022·2021-11-24
Tinactin Tolnaftate Liquid Spray Recalled for Benzene Contamination
Bayer Healthcare Pharmaceuticals is recalling Tinactin (Tolnaftate 1%) liquid spray due to the presence of benzene chemical contamination. The product was distributed nationwide through retail channels.
Product
TINACTIN — TINACTIN (TOLNAFTATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0249-2022·2021-11-24
Lotrimin Daily Prevention Deo Tolnaftate Spray Recalled for Benzene Contamination
Bayer Healthcare Pharmaceuticals is recalling Lotrimin Daily Prevention Deo (Tolnaftate 1%) spray powder due to the presence of benzene contamination. The recall affects 579,456 cans distributed nationwide.
Product
LOTRIMIN DAILY PREVENTION DEO — LOTRIMIN DAILY PREVENTION DEO (TOLNAFTATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0250-2022·2021-11-24
Tinactin Tolnaftate Deodorant Powder Spray Recalled for Benzene Contamination
Bayer Healthcare Pharmaceuticals is recalling Tinactin (Tolnaftate 1%) Deodorant Powder Spray due to the presence of benzene chemical contamination. The recall affects 738,432 cans distributed nationwide and internationally.
Product
TINACTIN — TINACTIN (TOLNAFTATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0233-2022·2021-11-24
Arrow-Trerotola Percutaneous Thrombolytic Device inner lumen detachment and embolization risk
Arrow-Trerotola PTD catheters are being recalled because the inner lumen can detach from the device basket, causing embolization that requires additional intervention. 1,167 units are affected.
Product
Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-65709-W The Arrow-Trerotola" Percutaneous Thrombolytic Device (PTDTM) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venousf
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0202-2022·2021-11-24
EveryPlate Meal Kits Recalled for Salmonella Contamination Risk
EveryPlate meal kits from production week 08/04/2021 are being recalled because they contain onions contaminated with Salmonella Oranienburg. The onions were purchased from ProSource.
Product
EveryPlate Meal Kit Product Codes 81-82-84-90-92-95-98-99 from Production Week 32 (production week start date: 08/04/2021)
Category
Food
Distribution
Distributed nationwide

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8751–8775 of 36629