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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 12,221–12,240 of 18,116 recalls

FDA Recall United States Terminated Historical recordClass III

Give and Go Prepared Foods Corp - Finch

Product
Two-Bite Turtle Brownie Party Platter 16 x 12.2 oz (346g) it…
Reason
Dried weevil larvae may be present in the recalled products.
Published
April 5, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Give and Go Prepared Foods Corp - Finch

Product
Two-Bite Pecan Tart 9.2 oz (261g) item number 02023; NL Two-…
Reason
Dried weevil larvae may be present in the recalled products.
Published
April 5, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Desonide Ointment, 0.05%, NET WT 60 grams tubes, Rx only, E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc., Melville, New York 11747, NDC 0168-0309-60

by Fougera Pharmaceuticals Inc.

Reason
Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may contain tubes of Desonide Ointment labeled as Ketoconazole Cream
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate Injection , USP, 200 mg/mL, 1 mL vial , For Intramuscular Use Only, Rx Only, Distributed by Sun Pharma Ind. Inc., NJ 08512, Manufactured by Sun Pharma Ind. Ltd. India, NDC 62756-015-40

by Sun Pharmaceutical Industries, Inc.

Reason
Presence of Particulate Matter
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Famciclovir tablets, 500 mg, packaged in 30-count unit dose cartons, Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-307-13

by AVKARE Inc.

Reason
Failed impurities/ degradation specifications: Product was above specification for unknown impurities.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 900 mg/180 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-190-30).

by PFIZER INC

Reason
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 750 mg/150 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-205-25).

by PFIZER INC

Reason
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 300 mg/60 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-190-10).

by PFIZER INC

Reason
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

ATENOLOL Tablets, USP, 50 mg, 30-count bottle, Rx only, Distributed by: The Kroger Co., 1014 Vine Street, Cincinnati, OH 45202; Manufactured for: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534; Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045; NDC 68645-493-54.

by Legacy Pharmaceutical Packaging LLC

Reason
Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC 68382-023-10), Rx only, Manufactured by: Cadila Healthcare Ltd., India; Distributed by: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534.

by Zydus Pharmaceuticals USA Inc

Reason
Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dolce Dolci LLC dba Villa Dolce Gelato

Product
Strawberry Sorbet, 5 Liter, 1 unit/case
Reason
Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto because they have the potential to be contaminated with hepatitis A virus.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dolce Dolci LLC dba Villa Dolce Gelato

Product
Strawberry Gelato, 5 Liter, 1 unit/case
Reason
Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto because they have the potential to be contaminated with hepatitis A virus.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Manzana Products Co., Inc.

Product
Trader Joe's All Natural Unsweetened Apple Sauce; 24 oz. gl…
Reason
Manzana Products Co. is initiating a recall of three varieties of apple sauce after receiving customer complaints or finding small pieces of glass in the product.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Manzana Products Co., Inc.

Product
Trader Joe's First Crush Unsweetened Gravenstein Apple Sauce…
Reason
Manzana Products Co. is initiating a recall of three varieties of apple sauce after receiving customer complaints or finding small pieces of glass in the product.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Manzana Products Co., Inc.

Product
Trader Joe's Organic Unsweetened Apple Sauce; 24 oz. glass…
Reason
Manzana Products Co. is initiating a recall of three varieties of apple sauce after receiving customer complaints or finding small pieces of glass in the product.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Diamond Crystal Brands Inc

Product
Natural Cocoa Powder 22-24% cocoa butter, Net Wt. 5 lbs. (2.…
Reason
During sanitation, the firm discovered metal pieces missing from a sifter screen.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Diamond Crystal Brands Inc

Product
Natural Cocoa Powder 10-12% cocoa butter, Net Wt. 5 lbs. (2.…
Reason
During sanitation, the firm discovered metal pieces missing from a sifter screen.
Published
March 29, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Diamond Crystal Brands Inc

Product
Baking Powder Net Wt. 5 lbs. (2.27 kg) packaged 6 bags per c…
Reason
During sanitation, the firm discovered metal pieces missing from a sifter screen.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Life Rising Corp S

Product
Life Rising TT Side Head Regulator, Chinese Herbal Supplemen…
Reason
High levels of lead discovered in product.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Buffered Lidocaine, 1%, In Sodium Bicarbonate 8.4%, 1 mL Total Volume in a 3 mL syringe, Local anesthetic use, Rx only, PharMEDium, Product code 2K2466

by PharMEDium Services, LLC

Reason
Labeling; Label Mixup; outer packaging is incorrectly labeled as Buffered Lidocaine 1% instead of correctly as Buffered Lidocaine 0.9%
Published
March 22, 2017
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.