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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,063

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls

Most common hazardLack of Assurance of Sterility 2,072 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 2026

Most affected stateHawaii 200 recalls mention this state

State: GA ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 11, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Terminated Historical recordClass II

M&S Dental Supply Co LLC., Topical Anesthetic Gel, Benzocaine 20%, Net Wt. 1 oz. (30ml), Manufactured for: M&S Dental Supply Co LL, 105-30 101 Avenue, Ozone Park, NY 11416.

by Keystone Industries

Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.
Published: December 25, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Gelato, Benzocaine 20% Topical Gel Anesthetic Gel, Net Wt. 1 oz. (30ml), Manufactured by Keystone Industries 480 S. Democrat Rd., Gibbstown, NJ 08027, NDC# 68400-352-30.

by Keystone Industries

Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.
Published: December 25, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS LTD

Product: Item 16354301, MAXI - 44067705 - MAXI KR BA BA 3040 EX, 55.1…
Reason: potential for pieces of metal in product
Published: December 25, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS LTD

Product: Item 25293502, ADHESION BREADER EX, 50 lb. bag
Reason: potential for pieces of metal in product
Published: December 25, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS LTD

Product: Item 79588401, ITAL STY PD HERB REDUCED EX, 55 lb. bag
Reason: potential for pieces of metal in product
Published: December 25, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS LTD

Product: Item 18968101, 100138 ITALIAN MBALL DRY MIX EX, 40.84 lb. ba…
Reason: potential for pieces of metal in product
Published: December 25, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS LTD

Product: Item 42081001, 104023600 SPICY BREADING EXPORT, 50 lb. bag
Reason: potential for pieces of metal in product
Published: December 25, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

Terry and Joe Baker Farms, Llc dba Baker Farms

Product: Baker Farms CURLY MUSTARD 16 oz NET WT 16 oz UPC 8 13098 020…
Reason: The firm was notified by the Texas Department of Agriculture that the product test positive for Listeria monocytogenes.
Published: December 25, 2024
Distribution: Product was shipped to distribution cent…

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FDA Recall United States Terminated Historical recordClass II

Yoder's Cashew Crunch

Product: Yoder's Cashew Crunch Corn, bulk candy coated popcorn packag…
Reason: Undeclared allergen labeling (milk)
Published: December 25, 2024
Distribution: Distributed to retail and wholesale in:…

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FDA Recall United States Terminated Historical recordClass II

Yoder's Cashew Crunch

Product: Candy coated popcorn packaged in clear plastic with gold lab…
Reason: Undeclared allergen labeling (milk)
Published: December 25, 2024
Distribution: Distributed to retail and wholesale in:…

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FDA Recall United States Terminated Historical recordClass II

Yoder's Cashew Crunch

Product: Yoder's Cashew Crunch, hard candy shipped in bulk in clear p…
Reason: Undeclared allergen labeling (milk)
Published: December 25, 2024
Distribution: Distributed to retail and wholesale in:…

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FDA Recall United States Terminated Historical recordClass II

Yoder's Cashew Crunch

Product: Hard candy packed in clear plastic bag with gold/red label,…
Reason: Undeclared allergen labeling (milk)
Published: December 25, 2024
Distribution: Distributed to retail and wholesale in:…

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FDA Recall United States Terminated Historical recordClass II

Yoder's Cashew Crunch

Product: Hard candy packed in clear plastic bag with gold/red label,…
Reason: Undeclared allergen labeling (milk)
Published: December 25, 2024
Distribution: Distributed to retail and wholesale in:…

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FDA Recall United States Terminated Historical recordClass I

Fabalish,

Product: Fabalish Inc. , Kickin, Carrot Falafel , 10oz , Cardboard t…
Reason: Potential E Coli contamination.
Published: December 25, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Impossible Foods Inc

Product: Impossible Spicy Ground Sausage Meat from plants 14oz chub,…
Reason: product may contain pieces of metal
Published: December 25, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Impossible Foods Inc

Product: Impossible Savory Ground Sausage Meat from plants 14oz chub,…
Reason: product may contain pieces of metal
Published: December 25, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 42292-040-20

by Mylan Institutional, Inc.

Reason: Subpotent and Superpotent Drug
Published: December 18, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 150 mcg (0.150 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 51079-445-20

by Mylan Institutional, Inc.

Reason: Subpotent and Superpotent Drug
Published: December 18, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 137 mcg (0.137 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 42292-041-20

by Mylan Institutional, Inc.

Reason: Subpotent and Superpotent Drug
Published: December 18, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 51079-443-20

by Mylan Institutional, Inc.

Reason: Subpotent and Superpotent Drug
Published: December 18, 2024
Distribution: Nationwide

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Data last updated: September 11, 2026 ET

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.