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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.

37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 4,041–4,060 of 18,690 recalls

FDA Recall United States Terminated Historical recordClass I

Tai Phat Wholesalers LLC

Product
Three Gold Coins, Dried Mushrooms Sliced (01276) Nam Meo S…
Reason
Products were found to be contaminated with Salmonella.
Published
January 11, 2023
Distribution
The product was distributed to consignee…

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FDA Recall United States Terminated Historical recordClass I

Tai Phat Wholesalers LLC

Product
Three Gold Coins, Dried Mushrooms Sliced (01051) Nam Meo S…
Reason
Products were found to be contaminated with Salmonella.
Published
January 11, 2023
Distribution
The product was distributed to consignee…

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FDA Recall United States Terminated Historical recordClass I

Cranberry Sweets & More Inc

Product
Recalled Meltaways product is packaged in clear cellophane b…
Reason
Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is undeclared.
Published
January 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Timolol Maleate Ophthalmic Solution, USP 0.5%, 2.5 mL, Rx Only, Mfg by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Mfg for: Apotex Corp. Weston, FL 33326, NDC 60505-1005-4

by Apotex Corp.

Reason
Failed Stability Specifications: Out of specification for weight loss at the 18-month stability timepoint and projected weight loss of 21.1% at shelf life.
Published
January 4, 2023
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Alcohol Antiseptic 80% Topical Solution Hand Sanitizer, Non-Sterile Solution, packaged as a a) 2.5 gallon bottle (9,464 ml), NDC 55533-524-02, and b) 55 gallon bottle (208,198 ml), NDC 55533-524-03, Manufactured for: Multi-Mist Products A Division of NCH Corporation 1618 Northgate, Irving, Texas 75062

by NCH Life Sciences LLC

Reason
CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in the product in excess of allowed limits.
Published
January 4, 2023
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Glycopyrrolate Tablets, USP, 1 mg, 50 Tablets (5x10) Unit Dose carton, Rx Only, Manufactured for: AvKARE Pulaski, TN 38478, NDC 50268-363-15

by AVKARE LLC

Reason
Failed impurities/degradation specifications: Out of specification for unknown impurities.
Published
January 4, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ganciclovir for Injection, USP, 500mg per vial, packaged in a 10-count carton, Rx Only, Mfd. by: THYMOORGAN PHARMAZIE GmbH, Germany, Distributed by Hikma Berkeley Heights, NJ 07922, NDC 0143-9299-01

by Hikma Pharmaceuticals USA Inc.

Reason
Labeling: Label mix-up - one vial was mislabeled as Cladribine Injection 10mg/mL inside a 10-count carton of Ganciclovir 500 mg.
Published
January 4, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Quinapril Tablets USP, 20 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, by: Lupin Limited, Goa 403 722 India, NDC# 68180-558-09

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
Published
December 28, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Quinapril Tablets USP, 40 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, by: Lupin Limited, Goa 403 722 India, NDC# 68180-554-09

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
Published
December 28, 2022
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Glycopyrrolate Tablets, USP, 1 mg, 100 tablets, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC 13107-014-01

by Aurolife Pharma, LLC

Reason
Failed Impurities/Degradation Specifications
Published
December 28, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Oxcarbazepine Tablets 600mg, packaged in a) 100- count bottles (NDC 62756-185-88), b) 500-count bottles (NDC 62756-185-13), c)1000-count bottles (NDC 62756-185-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Limited Halol-Baroda Highway, Halol-389 350, Gujarat, India.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Presence of foreign substance
Published
December 28, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Tri-Union Frozen Products Inc

Product
King Oscar Anchovies Flat Fillet in Olive Oil 2 oz. can 18 c…
Reason
Anchovies found to have elevated levels of histamine
Published
December 28, 2022
Distribution
Product was distributed to 2 DC's. DOT…

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FDA Recall United States Terminated Historical recordClass II

It'll Be Pizza, LLC.

Product
Take 2 Classic 18 oz, 24 ct/case; Take 2 Classic 20 oz, 22 c…
Reason
Product may be contaminated with foreign object (debris from packaging).
Published
December 28, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

It'll Be Pizza, LLC.

Product
20 oz Garlic and 24 oz Garlic frozen pizza dough manufacture…
Reason
Product may be contaminated with foreign object (debris from packaging).
Published
December 28, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

It'll Be Pizza, LLC.

Product
22 oz Blonde; 20 oz Blonde EZ; 24 oz Blonde EZ frozen pizza…
Reason
Product may be contaminated with foreign object (debris from packaging).
Published
December 28, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

It'll Be Pizza, LLC.

Product
24 oz Beer, frozen pizza dough manufactured by It'll Be Pizz…
Reason
Product may be contaminated with foreign object (debris from packaging).
Published
December 28, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

It'll Be Pizza, LLC.

Product
Circle K 22 oz Blonde Pizza Dough balls, 20 ct/case; frozen…
Reason
Product may be contaminated with foreign object (debris from packaging).
Published
December 28, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

It'll Be Pizza, LLC.

Product
EGA 22 oz Pizza Dough Ball, 20 ct/ case; frozen pizza dough
Reason
Product may be contaminated with foreign object (debris from packaging).
Published
December 28, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

It'll Be Pizza, LLC.

Product
Brava, 20 oz, 22 ct/case and Brava, 24 oz, 18 ct/case frozen…
Reason
Product may be contaminated with foreign object (debris from packaging).
Published
December 28, 2022
Distribution
Multiple states

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FDA Recall Terminated Historical recordClass III

Lacosamide Oral Solution, USP, CV, 10mg/mL, packaged in 200 mL bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Manufactured By: HETERO LABS LIMITED, Jeedimetla, Hyderabad - 500 055, India, NDC 31722-627-26

by Camber Pharmaceuticals, Inc

Reason
Failed Excipient Specifications: out of specification result observed for p-Hydroxybenzoic Acid content
Published
December 21, 2022
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.