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

6401–6425 of 7498

SevereFDA (Devices)·Z-0624-2022·2022-02-23
Teleflex Arrow-Trerotola Percutaneous Thrombolytic Device PTD Kit recalled for tip separation
Teleflex recalls approximately 1,400 Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) kits due to reports of tip separation during use. The medical device is used for dialysis graft declotting and has been distributed worldwide.
Product
Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-HFWC containing components: PT-65709-C, PT-03009, PT-65709-HFS The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0631-2022·2022-02-23
365 SKINNY High Intensity Capsules Recalled for Undeclared Sibutramine
Je Dois Lavoir LLC is recalling 365 SKINNY High Intensity Capsules (600 mg, 30-count bottles) because the product contains undeclared sibutramine, a drug previously withdrawn from the US market due to safety concerns.
Product
365 SKINNY High Intensity Capsules, 600 mg, 30-count bottle, BODY BALANCE INTERNACIONAL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0634-2022·2022-02-23
Morphine Sulfate Syringe Recall Due to Labeling Mix-Up
STAQ Pharma is recalling a limited number of syringes labeled as Morphine Sulfate PF that actually contain HYDROmorphone HCl PF due to a labeling error. The affected lot was distributed to Colorado, Ohio, and Texas.
Product
Morphine Sulfate PF 25 mg/25mL (1 mg/mL) in NaCl, 25 mL in 30 mL Single Dose Syringe, Rx only, STAQ Pharma, Inc., Denver, CO 80239, NDC: 73177-0105-04.
Category
Drug
Distribution
3 states
SevereFDA (Drugs)·D-0643-2022·2022-02-23
Paragard T380A Intrauterine Contraceptive Device Recall for Non-Sterility
CooperSurgical, Inc is recalling 48,645 cartons of Paragard T380A intrauterine contraceptive devices nationwide due to non-sterility concerns. The voluntary recall affects Lot #517001 with expiration date 1/2024.
Product
PARAGARD T380A (intrauterine copper contraceptive), 1 unit per carton together with an insertion tube and solid white rod in a Tyvek polyethylene pouch, Rx Only, Manufactured by Teva Women's Health Inc. a subsidiary of Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 51
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V104000·2022-02-23
Tesla Model S Side Curtain Air Bag Inflator Defect
Tesla is recalling 2021-2022 Model S vehicles due to side curtain air bag inflators that may have been assembled incorrectly. This could cause delayed air bag deployment during a crash, increasing injury risk.
Product
TESLA — 2022 TESLA MODEL S
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0626-2022·2022-02-23
Arrow-Trerotola Percutaneous Thrombolytic Device Kits Recalled for Tip Separation
Teleflex is recalling Arrow-Trerotola Percutaneous Thrombolytic Device kits worldwide due to reports of tip separation during use, affecting approximately 1,874 units.
Product
Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-WC containing components: PT-65709-C, PT-03009, PT-65709-HS The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits me
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0625-2022·2022-02-23
Arrow-Trerotola Dialysis Catheter Recalled for Tip Separation During Use
Arrow-Trerotola Over-The-Wire PTD catheters used in dialysis procedures are being recalled due to reports of tip separation during use. The FDA classified this as a Class I recall affecting 1,265 units worldwide.
Product
Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component: PT-65709-C The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of nati
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0563-2022·2022-02-23
MAC DADDY PURPLE Capsules Recalled for Undeclared Drug Ingredients
ABC Sales 1 Inc is recalling MAC DADDY PURPLE Capsules because they contain undeclared tadalafil and/or sildenafil, active ingredients in FDA-approved prescription drugs, making the product an unapproved drug.
Product
MAC DADDY PURPLE Capsules, packaged in 10-count blisters per carton, ASIN B08Z63Z4QK, UPC 742137 605764.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0633-2022·2022-02-23
HYDROmorphone HCl syringe recalled due to labeling mix-up
STAQ Pharma is recalling HYDROmorphone HCl PF syringes (lot 21104221A) that were incorrectly labeled as Morphine Sulfate PF. The mislabeling affects approximately 905 syringes distributed in Colorado, Ohio, and Texas.
Product
HYDROmorphone HCl PF 10 mg/50 mL (0.2mg/mL) in NaCl, 50 mL in 50 mL Single Dose Syringe, Rx only, STAQ Pharma, Inc., Denver, CO 80239, NDC: 73177-0104-05.
Category
Drug
Distribution
3 states
SevereFDA (Devices)·Z-0622-2022·2022-02-23
Vyaire Medical Ventilators Recalled Due to Potential Ventilation Failure
Vyaire Medical is recalling 4,189 bellavista 1000 and 1000e ventilators worldwide due to potential cessation of ventilation under specific conditions. This FDA Class I recall poses serious risk to patients who depend on these critical care devices.
Product
bellavista 1000 ventilator, Catalog #301.100.030 and bellavista 1000e ventilator, 301.100.130. The bellavista 1000/1000e ventilator is intended to provide positive pressure ventilatory support to adult and pediatric patients, and optionally, infant and neonatal patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0623-2022·2022-02-23
Arrow-Trerotola Thrombolytic Device Tip Separation During Use Recalled
Teleflex Medical is recalling Arrow-Trerotola PTD kits due to reports of tip separation during use. The affected device is used for declotting dialysis grafts and fistulae.
Product
Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-12709-WC, containing components: PT-12709-CA, PT-12709-C, The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0630-2022·2022-02-23
THE RED PILL EXTRA STRENGTH Capsules Recalled for Undeclared Tadalafil
THE RED PILL EXTRA STRENGTH 800 mg capsules are being recalled because they contain undeclared tadalafil, an active ingredient in FDA-approved sexual-enhancement medications. The product was marketed and distributed as an unapproved drug nationwide via Amazon.
Product
THE RED PILL, EXTRA STRENGTH capsules, 800 mg, packaged in 10-count blisters packaged in a carton, ASIN B0847BSQQ5, Barcode X002G5GMJ1.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V100000·2022-02-22
2021 Porsche Taycan: Center Seat Belt Buckle May Block Child Seat Anchors
Porsche is recalling 2020-2021 Taycan vehicles with optional rear center seats. The center seat belt buckle wiring harness may obstruct access to child seat anchors, preventing proper installation.
Product
PORSCHE — 2021 PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V091000·2022-02-17
2022 Chevrolet Corvette rear driveshaft defect may cause loss of power
General Motors is recalling 2021-2022 Chevrolet Corvette vehicles whose rear half-shaft assemblies may be missing ball bearings. This can cause sudden loss of drive power, increasing crash risk.
Product
CHEVROLET — 2022 CHEVROLET CORVETTE
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0698-2022·2022-02-16
Kroger Shredded Romaine Recalled for Potential Listeria Contamination
Dole Fresh Vegetables Inc is recalling Kroger 8oz Shredded Romaine (UPC 011110221483) due to potential Listeria monocytogenes contamination. The product was distributed across 36 states.
Product
Kroger 8oz Shredded Romaine Product UPC 011110221483
Category
Food
Distribution
36 states
CriticalFDA (Food)·F-0692-2022·2022-02-16
Kroger shredded green leaf recalled for potential Listeria contamination
Kroger 4.5oz shredded green leaf products are recalled for potential Listeria monocytogenes. Affected items have codes starting with N or Y and best-if-used-by dates from November 30, 2021 to January 8, 2022.
Product
Kroger 4.5oz Shredded Green Leaf Product UPC 011110061065
Category
Food
Distribution
36 states
CriticalFDA (Food)·F-0705-2022·2022-02-16
Marketside Cherry Almond Gorgonzola Chop Kit recalled for potential Listeria
Dole Fresh Vegetables is recalling Marketside Cherry Almond Gorgonzola Chop Kit for potential Listeria monocytogenes. Affected products have codes N or Y with Best if Used By dates from November 30, 2021 to January 8, 2022.
Product
Marketside 13.8oz Cherry Almond Gorgonzola Chop Kit Product UPC 681131305167
Category
Food
Distribution
36 states
CriticalFDA (Food)·F-0714-2022·2022-02-16
Dole Organic Baby Romaine Clamshells Recalled for Potential Listeria Monocytogenes
Dole Fresh Vegetables Inc is recalling two brands of 5oz organic baby romaine clamshells (Naturally Better and Nature's Promise) due to potential Listeria monocytogenes contamination. Products with specific date codes were distributed to 39 states.
Product
Naturally Better 5oz Organic Baby Romaine Clamshell Product UPC 607880203400 Nature's Promise 5oz Organic Baby Romaine Clamshell Product UPC 688267154485
Category
Food
Distribution
36 states
CriticalFDA (Food)·F-0675-2022·2022-02-16
Dole, Lidl, and Little Salad Bar chopped kits recalled for Listeria
Dole, Lidl, and Little Salad Bar chopped salad kits are being recalled due to potential Listeria monocytogenes contamination. Products were distributed to 38 US states.
Product
Dole 13.6oz Sesame Asian Chopped Kit Product UPC 071430000359 Lidl 12oz Sesame Asian Chopped Kit Product UPC 4056489210450 Little Salad Bar 12oz Chopped Asian Kit Product UPC 4099100086973
Category
Food
Distribution
36 states
CriticalFDA (Food)·F-0656-2022·2022-02-16
Dole Chopped Fiesta Lime Kit recalled for potential Listeria monocytogenes
Dole Fresh Vegetables is recalling Chopped Fiesta Lime Kit (10.7oz) for potential Listeria monocytogenes. Affected products have lot codes beginning with N or Y and best-if-used-by dates from November 30, 2021 to January 8, 2022.
Product
Dole 10.7oz Chopped Fiesta Lime Kit Product UPC 071430000991
Category
Food
Distribution
36 states
CriticalFDA (Food)·F-0691-2022·2022-02-16
Kroger Italian Blend Frozen Vegetables Recalled for Listeria Risk
Dole Fresh Vegetables Inc is recalling Kroger 10oz Italian Blend vegetables (UPC 011110910455) due to potential Listeria monocytogenes contamination. Affected products with Best if Used By dates between November 30, 2021 and January 8, 2022 were distributed across 38 states.
Product
Kroger 10oz Italian Blend Product UPC 011110910455
Category
Food
Distribution
36 states
CriticalFDA (Food)·F-0711-2022·2022-02-16
Spinach arugula blend recalled for potential Listeria monocytogenes
Dole is recalling Marketside Organic Spinach Arugula Blend due to potential Listeria monocytogenes contamination affecting approximately 2.3 million cases.
Product
Marketside 5oz Organic Spinach Arugula Blend Clamshell Product UPC 681131532082
Category
Food
Distribution
36 states
CriticalFDA (Food)·F-0712-2022·2022-02-16
Marketside 6oz Baby Greens Recalled Due to Potential Listeria Monocytogenes
Dole Fresh Vegetables Inc is recalling Marketside 6oz Baby Greens for potential Listeria monocytogenes contamination. Products were distributed across 36 states with Best if Used By dates from November 30, 2021 to January 8, 2022.
Product
Marketside 6oz Baby Greens Product UPC 681131355025
Category
Food
Distribution
36 states
CriticalFDA (Food)·F-0694-2022·2022-02-16
Kroger Organic Power Greens Recall Due to Potential Listeria Contamination
Dole Fresh Vegetables Inc is recalling Kroger 5oz Organic Power Greens due to potential Listeria monocytogenes contamination. The recall affects approximately 2.3 million cases distributed across 43 states.
Product
Kroger 5oz Organic Power Greens Clamshell Product UPC 111110917331
Category
Food
Distribution
36 states
SevereFDA (Food)·F-0697-2022·2022-02-16
Kroger 8oz Field Greens recalled due to potential Listeria monocytogenes
Dole Fresh Vegetables Inc is recalling Kroger 8oz Field Greens due to potential Listeria monocytogenes contamination. Approximately 2.3 million cases distributed across 40 states are affected.
Product
Kroger 8oz Field Greens Product UPC 011110910424
Category
Food
Distribution
36 states

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6401–6425 of 7498