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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.

37,143
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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
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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 12,801–12,820 of 21,044 recalls

FDA Recall Terminated Historical recordClass III

bupPROPion HCL Extended-Release Tablets, USP (XL) 300 mg, 500-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. NDC: 0378-2009-05

by Mylan Pharmaceuticals Inc.

Reason
Failed Impurities/Degradation Specifications: Mylan Pharmaceuticals Inc. is conducting a voluntary recall due to related out of specification compound results obtained during routine stability testing.
Published
January 31, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

DOXOrubicin Hydrochloride Liposome Injection, 20 mg/10 ml (2 mg/mL), 10 mL Single Use Vial, Distributed by: Sun Pharmaceutical Industries , Inc. Cranbury, NJ 08512. Manufactured by: Sun Pharmaceutical Ind. Ltd. Halol-Baroda Highway. Halol-389 350, Gujarat, India. NDC 47335-049-40

by Sun Pharmaceutical Industries, Inc.

Reason
Lack Of Assurance Of Sterility
Published
January 31, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets, USP 600 mg, 6 x 2500 Tablets bulk packed in double polybag shipper packs for further packaging, Rx only, Manufactured by: Marksans Pharma Ltd., Plot No. L-82, L-83, Verna Indl. Estate, Verna, Goa - 403 722, India, NDC 25000-122-28.

by Marksans Pharma Inc.

Reason
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Published
January 31, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Major Certa-Vite Liquid 236 mL UPC 00904-5023-09
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Leader Liquid Multivitamin Supplement for Infants and Toddle…
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Rugby Poly-Vitamin w/ Iron Liquid 50 mL UPC 00536-8530-80
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Major Poly-Vita Drops w/ Iron 50 mL UPC 00904-5100-50
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Major Tri-Vita Drops 50 mL UPC 00904-6274-50
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Rugby Tri-Vitamin Liquid 1 2/3 fl. oz. (50 mL) UPC 00536-850…
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Major Poly-Vita Drops 50 mL UPC 00904-5099-50
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Rugby Polyvitamin Liquid 1 2/3 fl. oz. (50 mL) UPC 00536-845…
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Major D-Vita Drops 50 mL UPC 00904-6273-50
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Leader Liquid Vitamin D Supplement for Breastfed Infants 400…
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Rugby D3 Vitamin liquid 400 IU/1 mL dose 1 2/3 fl. oz. (50 m…
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Rugby Cerovite Liquid 236 mL UPC 00536-2790-59
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Rugby Calcionate Syrup 16 oz. UPC 00536-2770-85
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Major Ferrous Drop Iron Supplement 50 mL UPC 00904-6060-50
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Rugby FER Iron Liquid 50 mL UPC 00536-0710-80
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Rugby Ferrous Sulfate Elixir 473 mL UPC: 00536-0650-85
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product
Rugby Liquid Vitamin C Supplement 500 mg 118 mL UPC 00536-01…
Reason
Presence of yeast and potential contamination with B. cepacia.
Published
January 31, 2018
Distribution
MI

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.