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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.

37,142
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
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 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 II24,349
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 13,421–13,440 of 18,726 recalls

FDA Recall United States Terminated Historical recordClass II

Green Dirt Farm, LLC

Product
Green Dirt Farm "Ruby" blended milk cheese packaged in cases…
Reason
Product is contaminated with Staphylococcus aureus exceeding action limit of 10,000 cfu/g.
Published
December 14, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

HANDY SEAFOOD INCORPORATED

Product
Handy Seafood, Blue Crab Cake Mini, Mini Crab Cakes, 0.5oz p…
Reason
Handy Seafood states that they are initiating this recall of Blue Crab Cake Mini, Mini Crab Cakes due to Milk (due to Butter in the ingredient statement) and Anchovies (in the Worcestershire Sauce) were not declared in the allergens statement on the package.
Published
December 14, 2016
Distribution
Gloucester, MA. (product further distrib…

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FDA Recall United States Terminated Historical recordClass I

Calbee North America, LLC

Product
HARVEST SNAPS, SNAPEA CRISPS, BLACK PEPPER FLAVORED GREEN PE…
Reason
One lot of black pepper flavored green pea crisps may contain wasabi ranch flavored green pea crisps which contain milk which is not declared on the black pepper flavored product.
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

ASK Foods Inc

Product
Taste of Inspirations Classic Red Skin Potato Salad; Creamy…
Reason
A.S.K. Foods, Inc. of Palmyra, Pennsylvania is voluntarily recalling one lot of Taste of Inspirations Classic Red Skin Potato Salad because it may contain undeclared egg.
Published
December 14, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Safecor Health, LLC

Product
Safecor Vitamin B-1 (THIAMINE) 100 mg tablets NDC: 48433-01…
Reason
Box labeled Thiamine Hydrochloride instead of Thiamine Mononitrate
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

SSI-GoPicnic LLC

Product
GoPicnic Turkey Slices & Cheddar Cheese; 4 Individually Pack…
Reason
Bagel chips containing wheat gluten included in a meal labeled "gluten free."
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenazopyridine Hydrochloride Tablets, USP, 200 mg, 100 count bottles, Rx only, Manufactured for: Nationwide Laboratories LLC, Iselin, New Jersey 08830, NDC 42937-702-10.

by Nationwide Laboratories, LLC

Reason
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenazopyridine Hydrochloride Tablets, USP, 100 mg, 100 count bottles, Rx only, Manufactured for: Nationwide Laboratories LLC, Iselin, New Jersey 08830, NDC 42937-701-10.

by Nationwide Laboratories, LLC

Reason
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Salsalate Tablets, USP, 750 mg, packaged in a) 100 count bottles (NDC 42937-704-10); b) 500 count bottles (NDC 42937-704-18); and c) 1000 count bottles (NDC 42937-704-20); Rx only, Manufactured for: Nationwide Laboratories LLC, Iselin, New Jersey 08830.

by Nationwide Laboratories, LLC

Reason
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Salsalate Tablets, USP, 500 mg, packaged in a) 500 count bottles (NDC 42937-703-18); b) 100 count bottles (NDC 42937-703-10); and c) 1000 count bottles (NDC 42937-703-20); Rx only, Manufactured for: Nationwide Laboratories LLC, Iselin, New Jersey 08830.

by Nationwide Laboratories, LLC

Reason
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenazopyridine Hydrochloride Tablets, USP, 200 mg, 100 count bottles, Rx only, Manufactured for: Burel Pharmaceuticals, Inc., Richland, MS --- NDC 35573-306-10

by Burel Pharmaceuticals Inc

Reason
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenazopyridine Hydrochloride Tablets, USP, 100 mg, 100 count bottles, Rx only, Manufactured for: Burel Pharmaceuticals, Inc., Richland, MS --- NDC 35573-304-10

by Burel Pharmaceuticals Inc

Reason
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Indiomin MB URINARY ANTISEPTIC, ANTISPASMODIC Capsules, Each capsule contains: Methenamine 120 mg, Monobasic Sodium Phosphate 40.8 mg, Methylene Blue, 10 mg; Hyoscyamine Sulfate, 0.12 mg, 100 count, Rx only, Manufactured for: BUREL PHARMACEUTICALS, NDC 35573-315-10

by Burel Pharmaceuticals Inc

Reason
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

AZUPHEN MB URINARY ANTISEPTIC Capsules, Each capsule contains: Methenamine 120 mg, Monobasic Sodium Phosphate 40.8 mg, Phenyl Salicylate 36 mg, Methylene Blue 10 mg, Hyoscyamine Sulfate, 0.12 mg, 100 count bottles, Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS --- NDC 35573-314-10

by Burel Pharmaceuticals Inc

Reason
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

UROPHEN MB URINARY ANTISEPTIC Tablets, Each tablet contains: Methenamine 81.6 mg, Benzoic Acid 9.0 mg, Phenyl Salicylate 36 mg, Methylene Blue 10.8 mg, Hyoscyamine Sulfate 0.12 mg, 100 count bottles, Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS --- NDC 35573-307-10

by Burel Pharmaceuticals Inc

Reason
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

URAMIT MB URINARY ANTISEPTIC Capsules, Each capsule contains: Methenamine 118 mg, Monobasic Sodium Phosphate 40.8 mg, Phenyl Salicylate 36 mg, Methylene Blue 10 mg, Hyoscyamine Sulfate, 0.12 mg, 100 count bottles, Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS --- NDC 35573-300-10

by Burel Pharmaceuticals Inc

Reason
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

UROLET MB URINARY ANTISEPTIC, ANTISPASMODIC Tablets, Each tablet contains: Methenamine 81.6 mg, Monobasic Sodium Phosphate 40.8 mg, Phenyl Salicylate 36 mg, Methylene Blue, 10.8 mg; Hyoscyamine Sulfate, 0.12 mg, (a) 30 count (NDC 35573-302-30) and (b) 100 count bottles (NDC 35573-302-10), Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS

by Burel Pharmaceuticals Inc

Reason
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Hyolev MB URINARY ANTISEPTIC Tablets, Each tablet for oral administration contains: Hyoscyamine Sulfate 0.12 mg, Methenamine 81 mg, Methylene Blue 10.8 mg, Phenyl Salicylate 32.4 mg, Sodium Phosphate Monobasic 40.8 mg, 90 count bottles, Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS --- NDC 35573-301-90

by Burel Pharmaceuticals Inc

Reason
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Travoprost Ophthalmic Solution USP, 0.004%, a) 2.5 mL and b) 5 mL bottles, Rx only, FOR USE IN THE EYES ONLY, Made in India, Distributed by: Par Pharmaceutical Cos., Inc, Spring Valley, NY 10977

by Par Pharmaceutical, Inc.

Reason
Lack of Assurance of Sterility; damage to the internal portion of the dropper tip portion of the container
Published
December 7, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

purely elizabeth.

Product
Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz,…
Reason
Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.
Published
December 7, 2016
Distribution
Nationwide

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.