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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.

36,949
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,732
Class I recallsReasonable probability of serious health consequences
24,263
Class II recallsTemporary or medically reversible health consequences
2,873
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 2,071 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/foods-alive-recalls-organic-moringa-leaf-powder-because-possible-health-riskPublished September 4, 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.

Download CSV

Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,458 recalls have been announced year to date.
  • Aug 2026 was 53% 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 II24,263
Class I9,732
Class III2,873
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,263
Class I9,732
Class III2,873
Not Yet Classified1

Showing 381–400 of 17,260 recalls

FDA Recall United States Ongoing 2026 recordClass I

JOHN B SANFILIPPO & SONS INC

Product
Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar UPC…
Reason
potential presence of Salmonella
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

PS Seasoning & Spices, Inc.

Product
PSW21585 Save A Lot Bind 50#, Part #: 20009709. PS Seasoni…
Reason
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

PS Seasoning & Spices, Inc.

Product
Blackstone Parmesan Ranch Seasoning, Net Wt 7.3 oz (207g).…
Reason
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

PS Seasoning & Spices, Inc.

Product
Ellsworth Sour Cream + Onion Seasoning, Part #: 180000113.…
Reason
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Liposomal Sleep Spray. Dosage: 6 sprays Liquid. Packaging: A…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Liposomal B12 Spray. Dosage: 3 sprays Liquid. Packaging: Alu…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging:…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid. Packaging…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Liposomal Prenatal+Postnatal Liquid Multivitamin Drops - Iro…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Liposomal Women's Liquid Multivitamin Drops - Iron Free. Dos…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Liposomal Kids Liquid Multivitamin Drops. Dosage: 3mL Liquid…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Liposomal Collagen Booster. Dosage: 3mL Liquid. Packaging: A…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Liposomal Women's Liquid Multivitamin Drops with Iron. Dosag…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Liposomal Mens 50+ Liquid Multivitamin Drops. Dosage: 3mL Li…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Liposomal Mens Liquid Multivitamin Drops. Dosage: 3mL Liqui…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Liposomal Womens 50+ Liquid Multivitamin Drops. Dosage: 3ml…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
Joint Nourish. Dosage:2 tablespoons (30mL). Liquid. For Oral…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Ascend Laboratories, LLC, Metoprolol Succinate Extended-Release Tablets, USP, 25 mg* Rx Only, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-590-01.

by Ascend Laboratories, LLC

Reason
Failed Dissolution Specifications
Published
May 20, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Buprenorphine Hydrochloride, Injection, 0.3mg/mL, 5x1 mL Single Dose Vials, Rx only, Manufactured for: Endo USA, Malvern, PA 19855, NDC 42023-179-05.

by ENDO USA, Inc.

Reason
Crystallization; identified as Buprenorphine free base
Published
May 20, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Oasis Tears PF, Preservative-Free Lubricant Eye Drops, 10mL/0.34 Fl OZ Bottle, Sterile, Manufactured for: OASIS Medical, Inc., 514 S. Vermont Ave., Glendora, CA 91741, USA, Made in France, NDC 42126-6400-1.

by Oasis Medical, Inc.

Reason
Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.
Published
May 20, 2026
Distribution
Nationwide

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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.