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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,118

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026

Most affected stateHawaii 200 recalls mention this state

State: AS ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 19, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass II

Pepperidge Farm, Incorporated

Product: Pepperidge Farm Goldfish Baked Snack Crackers Flavor Blasted…
Reason: Pepperidge Farm has been notified by one of its ingredient suppliers that whey powder in a seasoning that is applied to four varieties of Goldfish crackers has been the subject of a recall by the whey powder manufacturer due to the potential presence of Salmonella.
Published: August 15, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

KRAFT HEINZ FOODS COMPANY

Product: Food Network Kitchen Inspirations Asian Style Sesame Ginger…
Reason: Consumer complaints of product spoilage. Per the manufacturer this issue is premature spoilage due to the presence of Lactic Acid producing bacteria.
Published: August 15, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

KRAFT HEINZ FOODS COMPANY

Product: Taco Bell Salsa Con Queso Mild 15oz retail jar UPC 2100002…
Reason: Product is at risk for growth of Clostridium botulinum
Published: August 15, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 200 mg in 100 mL (2 mg/mL), 100 mL Single Dose Flexible Container bag, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902; By: Claris Injectables Ltd., Gujarat, India, NDC a) 36000-002-10 and b) 36000-002-06.

by Renaissance Lakewood, LLC

Reason: Superpotent Drug: lots out of specification for elevated sodium chloride and fluconazole assay.
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 200 mg in 100 mL (2 mg/mL), 100 mL Single Dose Flexible Container bag, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902; By: Claris Injectables Ltd., Gujarat, India, NDC 36000-002-10.

by Renaissance Lakewood, LLC

Reason: Failed Stability Specifications: lot out of specification for elevated water vapor.
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 400 mg in 200 mL (2 mg/mL), 200 mL Single Dose Flexible Container bag, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902; By: Claris Injectables Ltd., Gujarat, India; NDC 36000-003-06.

by Renaissance Lakewood, LLC

Reason: Superpotent Drug and Failed Stability Specifications: lot out of specification for elevated sodium chloride and elevated water vapor.
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Doxycycline Hyclate Tablets, USP, 100 mg, Rx Only, 30 tablets, 3 x 10 unit dose Cartons, Mfd. by: West-Ward Pharmaceuticals Corp., Eatontown, NY 07724; Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 USA. NDC: 0904-0430-04

by MAJOR PHARMACEUTICALS

Reason: Failed Dissolution Specifications
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Doxycycline Hyclate Tablets, USP, 100 mg*. 500-count bottle, Rx only. Manufactured by: West-Ward Pharmaceuticals Corp. Eatontown, NJ 07724. NDC# 0143-2112-05.

by West-Ward Columbus Inc

Reason: Failed Dissolution Specifications:
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Doxycycline Hyclate Tablets, USP, 100 mg*. 50-count bottle, Rx only. Manufactured by: West-Ward Pharmaceuticals Corp. Eatontown, NJ 07724. NDC# 0143-2112-50.

by West-Ward Columbus Inc

Reason: Failed Dissolution Specifications:
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daptomycin for Injection, 500 mg per vial, packaged as 1 Single-dose vial per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-0106-01.

by Pfizer

Reason: Microbial Contamination of Sterile Products: Product associated with reports of adverse events indicative of infusion reactions related to microbiological contamination.
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Indomethacin Capsules, USP, 50 mg, 100-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854; By: Hetero, Hetero Labs Limited, Jeedimetla, Hyderabad - 500 055, India; NDC 31722-543-01.

by Hetero Labs, Ltd. - Unit III

Reason: Failed Tablet/Capsule Specifications: customer complaints of deformed, clumped, misshaped, melted or stuck together capsules.
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product: Garlic Cheese Crouton Seasoning 50 pound bag Item 8590862…
Reason: Potential presence of Salmonella due to use of recalled whey ingredient
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product: Deep Pan Pizza Dough 1 pound 4 oz bag, 24 units per carton…
Reason: Potential presence of Salmonella due to use of recalled whey ingredient
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product: Cold Dough Premix 6.8 pound bag, 6 units per carton Item 1…
Reason: Potential presence of Salmonella due to use of recalled whey ingredient
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product: Seasoned Crouton Seasoning N5 50 pound bag Item 100001114…
Reason: Potential presence of Salmonella due to use of recalled whey ingredient
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product: Romano Garlic Seasoning 50 pound bag Item 1000015205
Reason: Potential presence of Salmonella due to use of recalled whey ingredient
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product: Onion Garlic Seasoning 50 pound bag Item 1000025776
Reason: Potential presence of Salmonella due to use of recalled whey ingredient
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product: Italian Crouton Seasoning 50 pound bag Item 1000012969
Reason: Potential presence of Salmonella due to use of recalled whey ingredient
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product: Italian Crouton Seasoning 50 pound bag Item 1000017039
Reason: Potential presence of Salmonella due to use of recalled whey ingredient
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product: Herb Crouton Seasoning 50 pound bag Item 859021000
Reason: Potential presence of Salmonella due to use of recalled whey ingredient
Published: August 8, 2018
Distribution: Nationwide

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Data last updated: September 19, 2026 ET

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.