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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.

37,204
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,841
Class I recallsReasonable probability of serious health consequences
24,366
Class II recallsTemporary or medically reversible health consequences
2,892
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 2,073 recalls
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)

  • 1,714 recalls have been announced year to date.
  • Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (297).
  • 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 II24,366
Class I9,841
Class III2,892
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 14,901–14,920 of 21,652 recalls

FDA Recall United States Terminated Historical recordClass II

Woodland Foods

Product
D'Allesandro Woodland Foods De-stemmed Birdseye Chiles 1,…
Reason
Trace amounts of undeclared peanut found in product
Published
June 21, 2017
Distribution
OK, TX, WI, NJ, FL, WA, NY, LA, SD, IL,…

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FDA Recall Terminated Historical recordClass III

Acyclovir Tablets, USP, 800 mg, 100-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, by Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar - 509 301, India, NDC 31722-778-01

by Hetero USA Inc

Reason
Presence of Foreign Substance: human hair melded into tablet.
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 6 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only Rx Only, Manufactured by; Qualgen 14844 Bristol Park Blvd. Edmond, OK 73013 NDC: 69761-006-01.

by Qualgen

Reason
CGMP deviations- Lack of Quality Assurance
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 10 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only , For Subcutaneous Use Only Rx Only Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC: 69761-010-01

by Qualgen

Reason
CGMP deviations- Lack of Quality Assurance
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 12.5 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only, Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013, NDC: 69761-012-01

by Qualgen

Reason
CGMP deviations- Lack of Quality Assurance
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 15 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles. Sterile Office Use Only, For Subcutaneous Use Only, Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013, NDC: 69761-015-01

by Qualgen

Reason
CGMP deviations- Lack of Quality Assurance
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 18 mg pellet , 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, Subcutaneous Use Only, Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC: 69761-018-01.

by Qualgen

Reason
CGMP deviations- Lack of Quality Assurance
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 20 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count and 12 count bottles, Sterile Office Use Only, For Subcutaneous Use Only Rx Only, Manufactured by Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC: 69761-020-01

by Qualgen

Reason
CGMP deviations- Lack of Quality Assurance
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 22 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF, in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC 69761-022-01

by Qualgen

Reason
CGMP deviations- Lack of Quality Assurance
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 25 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF, in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only. Rx Only ,Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC 69761-025-01,

by Qualgen

Reason
CGMP deviations- Lack of Quality Assurance
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Option 2, Levonorgestrel Tablet, 1.5 mg, Emergency Contraceptive, 1 Tablet per box, Distributed By Perrigo, Allegan, MI 49010. NDC 0113-2003-12

by L. Perrigo Company

Reason
Defective Container: Carton is missing the tablet blister strip and tablet.
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Zenatane (isotretinoin) Capsules, USP, 40 mg, 30-count (3 x 10 Prescription Packs) per carton, Rx Only, Manufactured By: Cipla Limited, Kurkumbh Village, Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-137-81

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications: out of specification results observed for low dissolution.
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Zenatane (isotretinoin) Capsules, USP, 30 mg, 30-count (3 x 10 Prescription Packs) per carton, Rx Only, Manufactured By: Cipla Limited, Kurkumbh Village, Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-113-81

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications: out of specification results observed for low dissolution.
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Zenatane (isotretinoin) Capsules, USP, 20 mg, 30-count (3 x 10 Prescription Packs) per carton, Rx Only, Manufactured By: Cipla Limited, Kurkumbh Village, Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-136-81

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications: out of specification results observed for low dissolution.
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Zenatane (isotretinoin) Capsules, USP, 10 mg, 30-count (3 x 10 Prescription Packs) per carton, Rx Only, Manufactured By: Cipla Limited, Kurkumbh Village, Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-135-81

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications: out of specification results observed for low dissolution.
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Levonorgestrel, U.S.P. active pharmaceutical ingredient, packaged in 1 kg container, Rx only, Spectrum Chemical Mfg. Corp, Gardena, CA 90248, New Brunswick, NJ 08901, Product code L1229.

by Spectrum Laboratory Products, Inc.

Reason
CGMP Deviations: these repackaged and redistributed products are being recalled due to a recall notice from the active pharmaceutical ingredient manufacturer for deviations from current Good Manufacturing Practices that were found during a recent FDA inspection.
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol (17-B-Estradiol; Estra-1,3,5(10)-triene-3, 17B-diol; Oestradiol) Plant Base, Micronized, U.S.P active pharmaceutical ingredient, packaged in 1g, 5g, 25g, 6 x 25g, and 100g containers, Rx only, Spectrum Chemical Mfg. Corp, Gardena, CA 90248, New Brunswick, NJ 08901, Product code E1435.

by Spectrum Laboratory Products, Inc.

Reason
CGMP Deviations: these repackaged and redistributed products are being recalled due to a recall notice from the active pharmaceutical ingredient manufacturer for deviations from current Good Manufacturing Practices that were found during a recent FDA inspection.
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Fourth Street Barbeque, Inc.

Product
Pick 5 Chicken & Waffle Sandwich; Mix & Match, Keep Frozen;…
Reason
Product has the potential to be contaminated with Listeria monocytogenes.
Published
June 14, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Still Riding Foods, LLC

Product
STILL RIDING FOODS GLUTEN FREE PIZZA CRUST; Sold in the foll…
Reason
C. botulinum hazard in vacuum packaged pizza crust.
Published
June 14, 2017
Distribution
US: CA CO CT DC DE FL IA ID IL…

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FDA Recall United States Completed Historical recordClass II

Pinnacle Foods, LLC

Product
Mrs. Butter-worth's(R) ORIGINAL PANCAKES, 144 COUNT, NET WT…
Reason
Potential for Listeria monocytogenes contamination
Published
June 14, 2017
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.