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

9501–9525 of 36630

SevereFDA (Food)·F-0659-2021·2021-06-16
Organic Microwave Butter Popcorn Recall Due to Undeclared Milk
Gilster-Mary Lee Corp. is recalling Organic Microwave Butter Popcorn because butter microwave popcorn bags were packaged in organic salted popcorn consumer boxes, resulting in undeclared milk in the product. The recall affects 413 cases distributed to multiple states.
Product
Organic Microwave Butter Popcorn in cartons labeled to be Organic Microwave Popcorn Salted, Net Wt 8.7 OZ, Distributed by TOPCO Associates LLC Elk Grove, IL, UPC 0 36800 40611 7
Category
Food
Distribution
9 states
SevereFDA (Food)·F-0674-2021·2021-06-16
BC Foods Celery Stalk and Leaf Dice Recalled for Salmonella
BC Foods is recalling Celery Stalk and Leaf Dice due to an ingredient testing positive for Salmonella. The product was distributed to food manufacturers and distributors across eight states.
Product
BC Foods Celery Stalk and Leaf Dice 3/8, AD Sulfites, 11 lb. Poly lined bulk fiber carton. Item code: VCE1-D38-AXG-AB-AR
Category
Food
Distribution
8 states
SevereFDA (Devices)·Z-1834-2021·2021-06-16
Surgical procedure pack anesthetic mislabeled with wrong drug and strength
DeRoyal Angio Cath Removal Tray contains mislabeled anesthetic; the label indicates 1% Lidocaine but the tray actually contains 0.5% Bupivacaine. This FDA Class I recall affects 60 trays distributed in MS, VA, LA, and NY.
Product
DeRoyal Angio Cath Removal Tray, REF 89-9936.02
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1832-2021·2021-06-16
DeRoyal Pacemaker Tray Mislabeled With Wrong Anesthetic Concentration
DeRoyal is recalling surgical procedure packs due to mislabeling. The product contains 0.5% Bupivacaine but is labeled as 1% Lidocaine, creating a medication identification error.
Product
DeRoyal Pacemaker Tray Pgybk, REF 89-6360.06
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0673-2021·2021-06-16
BC Foods AD Celery Stalk Products Recalled for Salmonella
BCFoods, Inc. is recalling certain BC Foods AD Celery Stalk products because an ingredient tested positive for Salmonella. The affected products are sold in bulk fiber cartons to food service and manufacturing customers.
Product
BC Foods AD Celery Stalk Canners, 25 lb. Poly lined bulk fiber carton, item code VCES-TCA-BJA-AA-AB; BC Foods AD Celery Stalk Cross Cut, 25 lb. Poly lined bulk fiber carton, item code VCES-TC9-BQS-AC-AB; BC Foods AD Celery Stalk Cross Cut, 25 lb. Poly lined bulk fiber carton, it
Category
Food
Distribution
8 states
SevereFDA (Devices)·Z-1537-2021·2021-06-16
FDA Recalls Innova COVID-19 Self-Test Kits Due to Unauthorized Distribution
Innova Medical Group is recalling COVID-19 self-test kits distributed to customers outside an authorized clinical investigation. The recall affects 370 boxes of tests distributed nationwide and internationally.
Product
COVID-19 Self-Test Kit *** INNOVA *** 7T
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0664-2021·2021-06-16
Hy-Vee Chicken Street Taco Kit Recalled for Undeclared Egg Allergen
Hy-Vee is recalling Chicken Street Taco kits because the chipotle crema component contains undeclared egg, a major food allergen. The product was distributed to Hy-Vee stores across multiple states.
Product
Hy-Vee Chicken Street taco kit, Net Wt. 18 OZ, UPC 282503 212993.
Category
Food
Distribution
8 states
SevereNHTSA·21E051000·2021-06-14
Wallace Forge recalls medium duty adjustable mount couplers
Wallace Forge is recalling specific medium duty adjustable mount couplers that may uncouple due to excessive play, increasing crash risk.
Product
EQUIPMENT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V445000·2021-06-11
Host Campers Recalls 2019-2021 Trailers Due to Gas Leak Risk
Host Industries is recalling 2019-2021 Cascade, Rainier, Tahoe, and Mammoth trailers because a stove bolt may damage the seal, causing a gas leak and fire risk.
Product
HOST CAMPERS — HOST CAMPERS RAINIER, TAHOE, CASCADE, MAMMOTH
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1651-2021·2021-06-09
Alaris Infusion Pump Module Bezel Repair Parts Recalled for Separation Risk
FDA recalls 22 serviced Alaris Model 8100 infusion pump units with bezel components that may crack or separate, risking free flow, over-infusion, under-infusion, or treatment interruption. Units distributed to Indiana and Texas between September 2020 and February 2021.
Product
Alaris Infusion Pump Module, Model 8100, serviced/repaired by The Biomed Guys, with the impacted bezel repair part, TIPA-8100-4410 / Alaris 8100 Bezel.
Category
Medical Device
Distribution
2 states
CriticalFDA (Drugs)·D-0627-2021·2021-06-09
Pfizer Lidocaine and Bupivacaine Injection Label Mix-Up Recall
Pfizer has recalled 139,050 vials of injectable anesthetic medications due to a label mix-up: some vials labeled as Lidocaine contain Bupivacaine, and some labeled as Bupivacaine contain Lidocaine. Patients and healthcare providers should verify medication identity before use.
Product
LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0646-2021·2021-06-09
Giant Eagle Chicken Street Taco Kit recalled for undeclared egg allergen
Giant Eagle is recalling Chicken Street Taco Kit packages due to undeclared egg allergen. The affected product was distributed to stores in PA, WV, OH, and IN.
Product
Giant Eagle Chicken Street Taco Kit; 20 oz (1 lbs 4 oz) Individual Units, PLU Code beginning 256598 00000
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-1620-2021·2021-06-09
Leccurate SARS-CoV-2 Antigen Test Kit Recalled: Not FDA-Approved for U.S. Distribution
The Leccurate SARS-CoV-2 Antigen Rapid Test Kit is being recalled because it was not authorized, cleared, or approved for marketing in the United States. Approximately 8.4 million units were distributed worldwide, including to U.S. states and territories.
Product
Leccurate SARS-CoV-2, Antigen Rapid Test Kit (Colloidal Gold Immunochromatography), 1 test, IVD. for the qualitative detection of antigen SARS-CoV-2 in clinical samples (nasal swab).
Category
Medical Device
Distribution
5 states
SevereFDA (Drugs)·D-0626-2021·2021-06-09
Bupivacaine and Lidocaine Injection Vials Recalled for Label Mix-Up
Pfizer is recalling 163,957 vials of 0.5% Bupivacaine Hydrochloride Injection due to a label mix-up where some vials labeled as bupivacaine may contain lidocaine, and vials labeled as lidocaine may contain bupivacaine. The mix-up could lead to patients receiving the wrong local anesthetic.
Product
BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0633-2021·2021-06-09
Mahayograj Guggulu Dietary Supplement Recalled for High Lead Contamination
Garry N Sun USA Inc. is recalling Mahayograj Guggulu dietary supplement capsules and powder due to high lead levels detected in a consumer sample. The product was distributed across multiple U.S. states and Canada.
Product
Mahayograj Guggulu; 120 Vegetarian Capsules, 1/2 lb. bags of powder Dietary Supplement, 1030 Matley Lane, Unit A Reno, NV 89502 Serving size: 2 capsule Servings per container: 60 Proprietary Blend - 500 mg Certified Organic Distributed by Garry N Sun USA
Category
Food
Distribution
11 states
SevereCPSC·21150·2021-06-09
Klein Tools Non-Contact Voltage Tester Recalled for Shock Hazard
Klein Tools non-contact voltage testers (model NCVT-1) are recalled because the on/off button can fail to disengage, causing the tester to malfunction and potentially fail to detect live voltage. One shock injury has been reported.
Product
Klein Tools Non-Contact Voltage Tester Model NCVT-1
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·21V437000·2021-06-09
Karavan Recalls 2021 Move I 1500 Long Trailers Due to Axle Weld Defect
Karavan is recalling 2021 Move I 1500 Long trailers because improperly welded wheel spindles can break, causing the wheel to detach and increasing crash risk.
Product
KARAVAN — KARAVAN MOVE I 1500 LONG
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0645-2021·2021-06-09
Peppa Pig Chocolate Chip Cookies Recalled for Undeclared Egg Allergen
PRIMARY COLORS DESIGN CORP is recalling Peppa Pig brand chocolate chip cookies due to undeclared egg allergen on the packaging. The recall affects 294 boxes distributed in Georgia, lot number 091820.
Product
Peppa Pig brand chocolate chip cookies. One 7 oz bag per box- 6 boxes per case
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-1619-2021·2021-06-09
Leccurate COVID-19 Antibody Test Kit Recalled for Unauthorized U.S. Distribution
LEPU Medical has recalled the Leccurate SARS-CoV-2 Antibody Rapid Test Kit because it is not authorized, cleared, or approved for marketing in the U.S. Approximately 8.4 million units have been distributed worldwide.
Product
Leccurate SARS-CoV-2, Antibody Rapid Test Kit (Colloidal Gold Immunochromatography), 1 test, IVD. for qualitative detection of IgM and/or IgG antibodies to SARS-CoV-2 in human serum, plasma and venipuncture whole blood for use as an aid in identifying individuals with an adapti
Category
Medical Device
Distribution
5 states
SevereNHTSA·21V430000·2021-06-04
Highland Ridge RV Recalls Trailers with Propane Regulator Defect
Highland Ridge RV is recalling certain 2019-2021 fifth wheel and travel trailers because a propane regulator may fail, increasing fire risk.
Product
HIGHLAND RIDGE FW — HIGHLAND RIDGE FW, HIGHLAND RIDGE TT OPEN RANGE, SILVERSTAR, MESA RIDGE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V426000·2021-06-04
KZRV Sidewinder Recalled for Propane Regulator Fire Risk
KZRV is recalling 2018-2019 Sidewinder RVs because a propane regulator may fail, increasing pressure and fire risk.
Product
KZRV — KZRV SIDEWINDER
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·21147·2021-06-03
Fisher-Price Recalls Rock 'n Glide Soothers After Four Infant Deaths
Fisher-Price is recalling 4-in-1 Rock 'n Glide Soothers and 2-in-1 Soothe 'n Play Gliders due to reports of four infant deaths from suffocation.
Product
Fisher-Price 4-in-1 Rock 'n Glide Soothers and 2-in-1 Soothe 'n Play Gliders
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·21V423000·2021-06-03
GM Recalls 2019 Silverado and Sierra 1500 for Tire Sidewall Defect
General Motors is recalling 2019 Chevrolet Silverado 1500 and GMC Sierra 1500 vehicles because over-cured tires may develop sidewall breaks, risking sudden air loss and loss of vehicle control.
Product
GMC — GMC, CHEVROLET SIERRA 1500, SILVERADO 1500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V422000·2021-06-03
2021 GMC Acadia Fuel Supply Line Recall Due to Fire Risk
General Motors is recalling certain 2021 GMC Acadia vehicles due to improperly attached fuel supply lines. The lines may loosen or separate, causing fuel leaks and increasing the risk of fire.
Product
CADILLAC — CADILLAC, GMC XT5, XT6, ACADIA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V420000·2021-06-03
Sea-Doo Move I Extended 1500 Trailer Recalled for Wheel Spindle Weld Defect
Bombardier is recalling 2021 Sea-Doo Move I Extended 1500 trailers because improperly welded wheel spindles can break, causing the wheel to detach and increasing crash risk.
Product
SEA-DOO — SEA-DOO MOVE I EXTENDED 1500
Category
Vehicle
Distribution
Distributed nationwide

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9501–9525 of 36630