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

23651–23675 of 26081

SevereFDA (Devices)·Z-0231-2022·2021-11-24
Arrow-Trerotola Percutaneous Thrombolytic Device Inner Lumen Detachment Recall
The inner lumen of Arrow-Trerotola Over-The-Wire PTD catheters (7FR) can detach from the device, causing an embolism. This requires additional medical intervention and delays treatment.
Product
Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-12709-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 (Food)·F-0186-2022·2021-11-24
Hardies Onion Yellow Jumbo Recalled for Salmonella Contamination Risk
Hardies Fruit & Vegetable Co., LP is recalling Onion Yellow Jumbo packed in 5-pound boxes due to potential Salmonella contamination. Consumers should not consume the affected product.
Product
Onion Yellow Jumbo packed in a 5 pound cardboard box Product Code 2377
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0205-2022·2021-11-24
EveryPlate Meal Kits Recalled for Salmonella Contamination
HelloFresh is recalling specific EveryPlate meal kits containing onions from ProSource that are associated with a Salmonella Oranienburg outbreak. Affected product codes from production week 08/25/2021 are being recalled nationwide.
Product
EveryPlate Meal Kit Product Codes 87-88-89-90-91-94-101 from Production Week 35 (production week start date: 08/25/2021)
Category
Food
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-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 (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 (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-0182-2022·2021-11-24
Yellow onions recalled for potential Salmonella contamination
Brothers Produce of Dallas Inc is recalling 5 lb. boxes of yellow onions due to potential Salmonella contamination. The affected product was distributed in Texas.
Product
5 lb. boxes of yellow onions packaged in cardboard boxes
Category
Food
Distribution
0 states
SevereFDA (Drugs)·D-0248-2022·2021-11-24
Lotrimin AF Powder Spray Recalled for Benzene Contamination
Bayer Healthcare is recalling Lotrimin AF miconazole nitrate 2% powder spray due to the presence of benzene chemical contamination. The recall affects approximately 3.8 million cans distributed nationwide.
Product
LOTRIMIN AF, (Miconazole nitrate 2%), Powder Spray, NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-0544-2 UPC 3 11017 41025 7
Category
Drug
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-0180-2022·2021-11-24
Red Jumbo Onions Recalled for Potential Salmonella Contamination
JF Palmer & Sons Produce is recalling 1,040 bags of red jumbo onions due to potential Salmonella contamination. The affected onions were distributed to MN, TX, CA, and MD.
Product
Onions Red Jumbo, packaged in 25 pound bulk bags
Category
Food
Distribution
4 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
0 states
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-0242-2022·2021-11-24
Tinactin Tolnaftate Deodorant Powder Spray Recalled for Benzene Contamination
Bayer Healthcare is recalling Tinactin (Tolnaftate 1%) Deodorant Powder Spray due to potential benzene contamination. The product was manufactured at a facility where other lots tested positive for benzene.
Product
TINACTIN — TINACTIN (TOLNAFTATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0196-2022·2021-11-24
HelloFresh Meal Kit Recalled for Salmonella Oranienburg Contamination
HelloFresh has recalled meal kits containing onions from ProSource that are associated with a Salmonella Oranienburg outbreak. The affected products were produced in Week 35 (starting August 25, 2021) and distributed nationwide.
Product
HelloFresh Meal Kit Product Code 4-12-14-18-23-25-AA from Production Week 35 (production week start date: 8/25/2021)
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0190-2022·2021-11-24
HelloFresh Meal Kits Recalled for Salmonella Contamination
HelloFresh is recalling certain meal kits containing onions from ProSource that are associated with a Salmonella Oranienburg outbreak. The affected kits have Product Codes 2-5-8-9-16-19-21-22-23-24-25 from Production Week 29 (starting July 14, 2021) and were distributed nationwide.
Product
HelloFresh Meal Kit Product Code 2-5-8-9-16-19-21-22-23-24-25 from Production Week 29 (production week start date: 07/14/2021)
Category
Food
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
HighFDA (Devices)·Z-0218-2022·2021-11-24
Cordis SMART FLEX Biliary Stent System recalled for potential tip separation
Cordis is recalling the SMART FLEX 6x150 BIL biliary stent system due to potential separation of the distal tip. Approximately 26 units were distributed in the U.S. and Canada. Affected patients should contact their healthcare provider.
Product
SMART FLEX 6x150 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-0216-2022·2021-11-24
FDA Recalls SMART FLEX Biliary Stents Due to Distal Tip Separation Risk
Cordis Corporation is recalling 9 SMART FLEX 9x60 biliary stent units due to a potential for distal tip dislodgement or separation. The stents were distributed to patients in several U.S. states and Canada.
Product
SMART FLEX 9x60 BIL, 80cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-0253-2022·2021-11-24
REGARD Newborn Tray Recalled Due to Out-of-Spec Antiseptic Component
ROi CPS LLC is recalling REGARD Newborn Trays (lot 86453F) distributed in FL, LA, and MO because some units contain a povidone-iodine swabstick component manufactured out of specifications.
Product
REGARD Newborn Tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0227-2022·2021-11-24
Beaver Xstar Crescent Knife surgical blades may have incorrect bevel angle
Approximately 5950 Beaver Xstar Crescent Knife surgical blades may be packaged with the wrong bevel angle, potentially affecting proper surgical technique during cataract procedures.
Product
Beaver Xstar Crescent Knife, 2.5mm, 55 degrees, bevel down. Intended for or cataract surgery. REF#: 373809
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0172-2022·2021-11-24
Yellow Onions from Mexico Recalled for Potential Salmonella
Keeler Family Farms is recalling whole raw yellow onions imported from Chihuahua, Mexico, due to potential contamination with Salmonella Oranienburg. The onions were shipped between July 1 and August 25, 2021.
Product
Whole raw onions - YELLOW - 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 b
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0236-2022·2021-11-24
Syphilis Test Calibrator Recalled for False-Positive Reactivity Issues
Bio-Rad BioPlex 2200 Syphilis calibrator set (791 units, Lot 52953) is recalled due to elevated test reactivity that does not confirm with treponemal tests and potential early shelf-life failure causing measurement bias.
Product
BIO-RAD BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator Set CAL The BioPlex 2200 Syphilis Total & RPR Calibrator Set is intended for the calibration of the BioPlex 2200 Syphilis Total & RPR Reagent Pack.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0179-2022·2021-11-24
White Onions Recalled Due to Potential Salmonella Contamination
JF Palmer & Sons Produce is recalling white onions packaged in 50-pound bulk bags due to potential Salmonella contamination. The recall affects onions distributed to Minnesota, Texas, California, and Maryland.
Product
Onions White, Medium, Large, Jumbo, packaged in 50 pound bulk bags
Category
Food
Distribution
4 states
HighFDA (Food)·F-0160-2022·2021-11-24
Carolina Ingredients Beef Gravy Mix Recalled for Elevated Lead Levels
Carolina Ingredients is recalling Beef Gravy Mix (product code N715025) due to elevated lead levels found in some samples after lab testing. All affected product was shipped to a customer in Georgia.
Product
Carolina Ingredients Beef Gravy Mix Non-allergen N715025 Net Wt. 50 lbs. Mfr. By: Carolina Ingredients, LLC Rock Hill, SC 29730
Category
Food
Distribution
1 state

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23651–23675 of 26081