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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,060
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/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 1,341–1,360 of 20,917 recalls

FDA Recall Ongoing Historical recordClass II

Doxepin Hydrochloride Capsules, USP, 10 mg, 100 Capsules, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panela v 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-637-31

by Alembic Pharmaceuticals Limited

Reason
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules, USP, 60mg, 1,000-count bottles, Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Distributed by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922. NDC 51991-748-10.

by Breckenridge Pharmaceutical, Inc.

Reason
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above safety assessment limit
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

QUEEN BEE GARDENS

Product
Brand Name: Queen Bee Gardens Whipped Honey Huckleberry Inte…
Reason
Product may have small flakes of stainless steel in product.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

QUEEN BEE GARDENS

Product
Brand Name: Queen Bee Gardens Whipped Honey Pure. Intended u…
Reason
Product may have small flakes of stainless steel in product.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

QUEEN BEE GARDENS

Product
Brand Name: Queen Bee Gardens Whipped Honey Raspberry. Inte…
Reason
Product may have small flakes of stainless steel in product.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Lorazepam Injection, USP, 2 mg/mL, 25 x 1mL vials/carton, Rx Only, Manufactured by: Hikma Berkeley Heights, NJ 07922, NDC# 0641-6044-25

by Hikma Pharmaceuticals USA Inc.

Reason
Failed Impurities/Degradation Specifications: An out-of-Specification for total related compounds
Published
August 6, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Sucralfate Tablets, USP 1 gram, packaged in a) 100-count bottles NDC 29033-0003-01, and b) 500-count bottles, NDC 29033-0003-05), Rx Only, Manufactured by: Nostrum Laboratories, Inc., Kansas City, MO 64120.

by Nostrum Laboratories, Inc.

Reason
CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.
Published
August 6, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Cinacalcet Tablets 90 mg, 30-count bottles, Rx only, Manufactured by: Strides Pharma Science Ltd. Puducherry, India; Distributed by: Strides Pharma Inc. East Brunswick, NJ 08816, NDC 64380-885-04

by Strides Pharma, Inc.

Reason
Failed Dissolution Specifications.
Published
August 6, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4ml-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001, Made in Austria, Carton NDC- 60793-702-10 , Syringe NDC-60793-702-04

by Pfizer Inc.

Reason
CGMP Deviations; particulates identified during visual inspection
Published
August 6, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Bicillin L-A (penicllin G benzathine injectable suspension), 1,200,000 units per 2 mL, 2 mL-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001. Made in Austria, Carton NDC - 60793-701-10, Syringe NDC - 60793-701-02

by Pfizer Inc.

Reason
CGMP Deviations; particulates identified during visual inspection
Published
August 6, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, NDC 64980-514-05.

by FDC Limited

Reason
Defective Container: spike of the cap becomes lodged in the nozzle of the product bottle.
Published
August 6, 2025
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg, 100 Capsules bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL, 34108, United States, Manufactured by: Lupin Limited, Goa 103 722, INDIA, NDC 68180-755-01.

by Lupin Pharmaceuticals Inc.

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong expiry date as Feb.2027 instead of Jan.2027
Published
August 6, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Newly Weds Foods, Inc.

Product
Newly Weds E54564-BREADER X5-NET WT 25LBS
Reason
potential Listeria Monocytogenes Contamination
Published
August 6, 2025
Distribution
FL, ID, IL, KS, MO, NY, OR, TX, WA, WI a…

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FDA Recall United States Terminated Historical recordClass I

Newly Weds Foods, Inc.

Product
Newly Weds B90737-BREADER X1-NET WT 25LBS
Reason
potential Listeria Monocytogenes Contamination
Published
August 6, 2025
Distribution
FL, ID, IL, KS, MO, NY, OR, TX, WA, WI a…

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FDA Recall United States Terminated Historical recordClass I

Newly Weds Foods, Inc.

Product
Newly Weds B6AAK3-BREAD CRUMBS X1-NET WT 35LBS
Reason
potential Listeria Monocytogenes Contamination
Published
August 6, 2025
Distribution
FL, ID, IL, KS, MO, NY, OR, TX, WA, WI a…

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FDA Recall United States Terminated Historical recordClass I

Newly Weds Foods, Inc.

Product
Newly Weds B6229J-PIZZA CRISP-NET WT 35LBS
Reason
potential Listeria Monocytogenes Contamination
Published
August 6, 2025
Distribution
FL, ID, IL, KS, MO, NY, OR, TX, WA, WI a…

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FDA Recall United States Terminated Historical recordClass I

Newly Weds Foods, Inc.

Product
Newly Weds B62262-BREAD CRUMBS X1-NET WT 1200 LBS
Reason
potential Listeria Monocytogenes Contamination
Published
August 6, 2025
Distribution
FL, ID, IL, KS, MO, NY, OR, TX, WA, WI a…

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FDA Recall United States Terminated Historical recordClass I

Newly Weds Foods, Inc.

Product
Newly Weds B61672--BREAD CRUMBS X1-NET WT 35 LBS.
Reason
potential Listeria Monocytogenes Contamination
Published
August 6, 2025
Distribution
FL, ID, IL, KS, MO, NY, OR, TX, WA, WI a…

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FDA Recall United States Terminated Historical recordClass I

Newly Weds Foods, Inc.

Product
Newly Weds B61610-BREAD CRUMBS X1-NET WT 45 LBS
Reason
potential Listeria Monocytogenes Contamination
Published
August 6, 2025
Distribution
FL, ID, IL, KS, MO, NY, OR, TX, WA, WI a…

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FDA Recall United States Terminated Historical recordClass I

Newly Weds Foods, Inc.

Product
Newly Weds B61453-BREAD CRUMBS X1-NET WT 25 LBS
Reason
potential Listeria Monocytogenes Contamination
Published
August 6, 2025
Distribution
FL, ID, IL, KS, MO, NY, OR, TX, WA, WI a…

View recall →

Data last updated:

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.