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Recall totals

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

37,066

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 12, 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 United States Terminated Historical recordClass II

AMY'S KITCHEN INC.

Product: Amy's Kitchen Enchilada Verde Whole Meal 10 oz. 12 pk Item #…
Reason: L. mono contamination
Published: May 1, 2024
Distribution: U.S. distribution to the following: CA,…

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FDA Recall Completed Historical recordClass II

S.P.Labs, Thyroid, Full Strength, Rx only, For Manufacturing, Processing or Repackaging Use Only, Specialty Process Labs, Phoenix, AZ 85034, NDC 81305-500-01.

by Specialty Process Labs LLC

Reason: Failed Stability Specifications
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Sterile Diluent, HUMALOG U-100 (insulin lispro injection), HUMULIN R U-100 REGULAR (insulin human injection), Insulin Lispro Injection u-100, 10 mL, Use ONLY with Insulins listed on carton, Marketed by: Lilly USA, LLC, Indianapolis, IN 46285. NDC: 0002-0800-01

by Eli Lilly & Company

Reason: CGMP Deviations
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Digoxin Tablets, USP 62.5 mcg (0.0625 mg), 100-count bottles, Rx Only, Manufactured by: Novitium Pharma LLC, 70 Lake Drive, East Windsor, New Jersey 08520, NDC 70954-200-10

by Novitium Pharma LLC

Reason: Failed Impurities/Degradation Specifications
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Vancomycin Hydrochloride for Oral Solution, USP, 250 mg per 5 mL, packaged as (a) 80 mL bottle, NDC 69238-2261-3; (b) 150 mL bottle, NDC 69238-2261-7; (c)300 mL bottle, NDC 69238-2261-5; Rx only, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807

by Amneal Pharmaceuticals of New York, LLC

Reason: Superpotent Drug: Due to overfilling of drug powder
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass III

NEXLIZET (bempedoic acid and ezetimibe) tablets, 180 mg/10 mg, 30-count bottle, Rx only, Manufactured for: Esperion Therapeutics, Ann Arbor, MI 48108, NDC 72426-818-03

by Esperion

Reason: Failed dissolution specifications: out-of-specification bempedoic acid dissolution at the 0-month timepoint.
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

S.P Labs, Thyroid, USP, Rx only, For Manufacturing, Processing or Repackaging Use only, Specialty Process Labs, Phoenix, AZ, NDC #'s a) 81305-100-01, b)81305-100-02, c)81305-100-03

by Specialty Process Labs LLC

Reason: Failed Stability Specifications
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Atovaquone Oral Suspension USP, 750 mg per 5 mL sachets, 20 Units x 5 mL cartons, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, NDC 50268-086-12.

by AvKARE

Reason: Microbial contamination of a non-sterile product: potential Bacillus cereus contamination.
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Canadian Art Prints

Product: Tranquility & Teachings William Monague plate set, brand Ind…
Reason: Product has been recalled because it may exceed FDA guidance levels for leachable lead.
Published: April 24, 2024
Distribution: Plates were distributed in Canada and in…

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FDA Recall Ongoing Historical recordClass I

Methocarbamol Injection, USP 1000mg/10mL, (100mg/mL), 10 mL Single-Dose Vial packed 25 vials per carton, Rx Only, Mfd. in India for: Eugia US LLC. E. Windsor, NJ 08520, NDC 55150-223-10

by Eugia US LLC

Reason: Presence of Particulate Matter
Published: April 17, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Isotretinoin Capsules, USP 40mg, 30-count 3x10 blister packs per carton, Rx Only, Manufactured For: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054. Blister Pack NDC 0591-2436-45, Carton NDC 0591-2436-15

by Teva Pharmaceuticals USA, Inc

Reason: Superpotent Drug: The 3-month stability result for assay was found to be above specification limit
Published: April 17, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lansoprazole Delayed-Release Capsules USP, 15 mg, Acid reducer 24 Hour, Treats Frequent Heartburn, 14 capsules per bottle, Manufactured by: Natco Pharma Limited Kothur- 509 228, India, Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ. 08816. NDC 16571-742-41

by NATCO Pharma Limited

Reason: CGMP Deviations
Published: April 17, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rifampin Capsules USP, 300mg, 30-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited Aurangabad 431 210 India, NDC 6818-0659-06

by Lupin Pharmaceuticals Inc.

Reason: Subpotent Drug
Published: April 17, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Lidl US TRADING

Product: Deluxe brand Macarons Party Edition 35 pieces 455g (35 x 13g…
Reason: Undeclared Wheat, Soy, Egg, Milk, Tree Nuts (foreign language labeling)
Published: April 17, 2024
Distribution: Imported product directly shipped to a w…

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FDA Recall United States Terminated Historical recordClass I

Backstage Center DBA CTC Seller

Product: Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35…
Reason: The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.
Published: April 17, 2024
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product: PIES & SIDES SWEET POTATO CASSEROLE CONTAINS: EGG, MILK PIES…
Reason: During an inspection by NCDA, the firm was notified that the product label fails to list any ingredients.
Published: April 17, 2024
Distribution: Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product: PIES & SIDES STRAWBERRY PIE INGREDIENTS: STRAWBERRY PIE FILL…
Reason: During an inspection by NCDA, the firm was notified that the product label fails to list any sub ingredients.
Published: April 17, 2024
Distribution: Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product: PIES & SIDES SQUASH CASSEROLE CONTAINS: MILK, EGGS, SOY, FIS…
Reason: During an inspection by NCDA, the firm was notified that the product label fails to list any ingredients.
Published: April 17, 2024
Distribution: Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass I

Robeson Enterprises

Product: PIES & SIDES PUMPKIN PIE 10.5 oz INGREDIENTS: PUMPKIN FILLIN…
Reason: During an inspection by NCDA, the firm was notified that the product contains undeclared milk and eggs. The label fails to list any sub ingredients and the contain statement does not list milk or eggs.
Published: April 17, 2024
Distribution: Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product: PIES & SIDES DOT'S POTATO BAKE 2lb INGREDIENTS: IDAHO POTATO…
Reason: During an inspection by NCDA, the firm was notified that the label fails to list any sub ingredients.
Published: April 17, 2024
Distribution: Products were shipped to the following s…

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Data last updated: September 12, 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.