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Recall totals

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

37,063

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/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 11, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Ongoing Historical recordClass II

B Natural Organics, Organic Sunscreen, Broad Spectrum, SPF 30, 25% non-nano Zinc Oxide, a) Nude Tint Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1002-2; b) Tint Free Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1001-2; c) Tan Tint Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1003-2.

by KABANA SKIN CARE

Reason: cGMP deviations
Published: July 16, 2025
Distribution: Multiple states

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules, USP, 40mg, 30-count bottles, Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922. NDC 51991-750-33.

by Breckenridge Pharmaceutical, Inc.

Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Published: July 16, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Famciclovir Tablets, USP 500 mg, 30-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Manufactured by: Macleods Pharmaceuticals Ltd., Daman, India NDC# 33342-026-07.

by Macleods Pharmaceuticals Ltd

Reason: Presence of Foreign Substance- Black hair strand found attached to a tablet in a sealed bottle.
Published: July 16, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

C SWEET PASTRY LLC

Product: C Sweet Ghouribeh Rolls with date, sesame, & pistachios 10 o…
Reason: Undeclared wheat, soy, and sesame
Published: July 16, 2025
Distribution: MI

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FDA Recall United States Terminated Historical recordClass II

C SWEET PASTRY LLC

Product: C Sweet Maamoul with Pistachios 8 oz., UPC 721782348967
Reason: Undeclared soy, contains statement is present but does not list pistachios
Published: July 16, 2025
Distribution: MI

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FDA Recall United States Terminated Historical recordClass II

C SWEET PASTRY LLC

Product: C Sweet Ghouribeh with Pistachios 7 oz., UPC 852664042755
Reason: Undeclared soy, contains statement is present but does not list pistachios
Published: July 16, 2025
Distribution: MI

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FDA Recall United States Terminated Historical recordClass II

C SWEET PASTRY LLC

Product: C Sweet Sweet Kaak 12 oz., UPC 721782348912
Reason: Undeclared wheat
Published: July 16, 2025
Distribution: MI

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FDA Recall United States Terminated Historical recordClass II

C SWEET PASTRY LLC

Product: C Sweet Maamoul with Dates 8 oz., UPC 852664042694
Reason: Undeclared soy and wheat
Published: July 16, 2025
Distribution: MI

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FDA Recall United States Terminated Historical recordClass I

Weaver Nut Company, Inc

Product: Weaver Chocolates, D2645 - Nonpareil, Semi-Sweet Chocolate…
Reason: Undeclared Milk Allergen
Published: July 16, 2025
Distribution: The adulterated product was distributed…

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FDA Recall United States Terminated Historical recordClass I

Weaver Nut Company, Inc

Product: Weaver Chocolates, 47518 - Nonpareil, Semi-Sweet Chocolate…
Reason: Undeclared Milk Allergen
Published: July 16, 2025
Distribution: The adulterated product was distributed…

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FDA Recall United States Terminated Historical recordClass I

Lipari Foods Operating Company, LLC.

Product: JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plas…
Reason: Undeclared milk
Published: July 16, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units), For IV use, Sterile, Rx Only, Manufactured in Austria by Sandoz GmbH for Sandoz Inc. Princeton, NJ 08540, NDC: 0781-6136-94.

by Sandoz Inc

Reason: Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram were incorrectly labeled as penicillin G potassium for Injection, USP, 20 million Unit
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Cefazolin for Injection, USP, 1 gram per vial, Sterile, For Intramuscular or Intravenous Use, Rx Only, Manufactured by Sandoz GmbH for Sandoz Inc. Princeton, NJ 08540, NDC: 0781 3451-70 (vial), NDC: 0781-3451-96 (carton).

by Sandoz Inc

Reason: Labeling: Label Mix-Up; cartons of Cefazolin for Injection, USP 1 gram were found to contain vials labeled as penicillin G potassium for Injection, USP, 20 million Unit. The vials contained Cefozalin
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Pitavastatin Tablets, 2 mg, 90 Tablets per bottle, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC: 42291-906-90

by AvKARE

Reason: Failed Impurity/Degradation Specifications
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Pitavastatin Tablets, 1 mg, 90 Tablets per bottle, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC: 42291-905-90

by AvKARE

Reason: Failed Impurity/Degradation Specifications
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Metoprolol Succinate Extended-Release Tablets, USP, 25 mg, Packaged in a) 100-count bottle, NDC 70010-780-01; b) 500-count bottle, NDC 70010-780-05; Rx only, Manufactured by: Granules India Limited, Hyderadab-500 081, India, Manufactured for: Granules Pharmaceuticals Inc., Chantilly, VA 20151,

by Granules Pharmaceuticals Inc.

Reason: Failed Dissolution Specifications: Product failed to meet dissolution acceptance criteria in the stability studies at the 6th month (25¿C/60% RH) long-term.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Gabapentin Capsules, USP, 100 mg, 10 capsules (10x1) per bag, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN, 46268 USA, Distributed by Cardinal Health, Dublin, OH 43017, NDC 55154-3363-0

by The Harvard Drug Group LLC

Reason: Defective container; blister packaging inadequately sealed.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Gabapentin Capsules, USP, 100 mg, 100 capsules (10x10), blister pack cartons, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN, 46268 USA, NDC 0904-6665-61

by The Harvard Drug Group LLC

Reason: Defective container; blister packaging inadequately sealed.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Orajel Baby, Cooling Swabs for Teething, Each Unit 0.007 fl oz (0.22 mL), NET 0.08 FL OZ (2.6 mL) TOTAL, 12 Single-Use Swabs per carton, Manufactured for Church & Dwight Co. Inc. Ewing. NJ 08328 USA. UPC CODE 3 10310 40000 2.

by Church & Dwight Inc

Reason: Microbial Contamination of Non-Sterile Products: Fungal contamination of infant oral swabs.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

ZICAM NASAL ALLCLEAR, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc.., Ewing NJ. UPC 7 32216 30165 6

by Church & Dwight Inc

Reason: Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.
Published: July 9, 2025
Distribution: Nationwide

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Data last updated: September 11, 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.