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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 October 2026.

37,324
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,859
Class I recallsReasonable probability of serious health consequences
24,440
Class II recallsTemporary or medically reversible health consequences
2,900
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 2,095 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,440
Class I9,859
Class III2,900
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,440
Class I9,859
Class III2,900
Not Yet Classified2

Showing 4,101–4,120 of 19,414 recalls

FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Ceftriaxone for Injection, USP 500 mg per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC 66794-212-42

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Cefepime for Injection, USP 2 grams per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-090-02

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Ampicillin and Sulbactam for Injection, USP 3 grams vials, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-242-41

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Ampicillin and Sulbactam for Injection, USP 15 grams per Pharmacy Bulk Package, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-243-15

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Ampicillin and Sulbactam for Injection, USP 1.5 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-241-41

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Ampicillin and Sulbactam for Injection, USP 1.5 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-206-41

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Ampicillin and Sulbactam for Injection, USP 3 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-006-30

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Ampicillin and Sulbactam for Injection, USP 1.5 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-005-20

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Ampicillin for Injection, USP 1g per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-086-02

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Ampicillin for Injection, USP 2g per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-223-41

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Admelog, insulin lispro injection, 100 units/mL (U-100), 3mL multi-dose vial, Rx Only, Sanofi-Aventis U.S. LLC, Bridgewater, NJ 08807 A Sanofi Company. NDC 0024-5926-05

by Sanofi-Aventis U.S. LLC

Reason
Lack of Assurance of Sterility: Malformed crimped collar seal
Published
May 24, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: September 9, 2025Historical recordClass I

General Mills, Inc

Product
Gold Medal Bleached All Purpose Flour, Enriched, Presifted,…
Reason
Flour has the potential to be contaminated with Salmonella.
Published
May 24, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: September 9, 2025Historical recordClass I

General Mills, Inc

Product
Gold Medal Unbleached All Purpose Flour, Enriched, Presifted…
Reason
Flour has the potential to be contaminated with Salmonella.
Published
May 24, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: September 8, 2023Historical recordClass I

Lipari Foods Operating Company, LLC.

Product
Distributed by Lipari Foods Ground Cumin in 6oz plastic tub,…
Reason
Product tested positive for Salmonella
Published
May 24, 2023
Distribution
Retail stores throughout Alabama, Arkans…

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FDA Recall United States TerminatedTerminated: December 13, 2023Historical recordClass II

Big Bold Health Holdings Inc

Product
Microbiome Rejuvenate dietary supplement, 60 capsules per bo…
Reason
Glass fragments.
Published
May 24, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 30, 2024Historical recordClass III

Gabapentin Tablets, USP 600 mg, packaged in Cartons of 100 tablets (10 tablets per blister pack x 10), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. East Windsor, NJ 08520 Distributed by: Major Pharmaceuticals 17177 N Laurel Park Dr., Suite 233 Livonia, MI 48152 USA, NDC 0904-6823-61

by The Harvard Drug Group

Reason
Product mixup: one foreign tablet found in product.
Published
May 17, 2023
Distribution
Nationwide

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FDA Recall CompletedHistorical recordClass II

Calcitonin Salmon (synthetic origin) Nasal Spray, 2200 USP Calcitonin Salmon Units/mL, 200 USP Calcitonin Salmon Units/spray, 3.7 mL bottle, Rx only, Manufactured by: Apotex Corp., Toronto, Ontario, Canada, M9L 1T9, NDC 60505-0823-6

by Apotex Corp.

Reason
Presence of Foreign Substance: Glass splinter particle entrapped inside the pump ball seat rendered the pump inoperable.
Published
May 17, 2023
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

Atovaquone Oral Suspension USP, 750 mg/5 mL, Packaged in 210 mL bottle, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Manufactured by: Hetero Labs Limited, Jeedimetla, Hyderabad - 500 055, India, NDC# 31722-629-21.

by Camber Pharmaceuticals Inc.

Reason
Microbial Contamination of Non-Sterile Product: Objectionable organism, identified as Bacillus cereus, found in product during testing of repackaged product.
Published
May 17, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: September 19, 2023Historical recordClass I

Euro-Pharma

Product
Multiple Vitamin B Capsules, 60 Capsules, Biologically Activ…
Reason
undeclared allergen (milk)
Published
May 17, 2023
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: October 13, 2023Historical recordClass II

ZB Importing LLC

Product
Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker…
Reason
Elevated levels of lead
Published
May 17, 2023
Distribution
AL, AR, AZ, CA, CT, DE, FL, IA, IL, IN,…

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.

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