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Recall totals

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

37,115

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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 15, 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 I

Fudgeamentals LLC

Product: 1. Marketside FUDGE TRIO HOLIDAY FUDGE TRAY - 16 oz. 2. W…
Reason: made with peanut butter contaminated with Salmonella
Published: July 6, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product: PEANUT BUTTER FUDGE BAR (24-8OZ) FUDGEAMENTALS
Reason: made with peanut butter contaminated with Salmonella
Published: July 6, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product: PEANUT BUTTER FUDGE BITES (24-8 OZ) FUDGEAMENTALS
Reason: made with peanut butter contaminated with Salmonella
Published: July 6, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product: PEANUT BUTTER CHOCOLATE FUDGE BITES (24-8 OZ) FUDGEAMENTALS
Reason: made with peanut butter contaminated with Salmonella
Published: July 6, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product: VARIETY TRAY (16 OZ) (C-CNC-PBC) FUDGEAMENTALS
Reason: made with peanut butter contaminated with Salmonella
Published: July 6, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product: PEANUT BUTTER CHOCOLATE FUDGE BAR - 8 oz.
Reason: made with peanut butter contaminated with Salmonella
Published: July 6, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Tretinoin Capsules, 10 mg, Rx Only, 100 capsules per bottle, Teva Pharmaceuticals USA Inc., North Wales, PA, 19454, NDC 0555-0808-02.

by Teva Pharmaceuticals USA Inc

Reason: Failed Dissolution Specifications; Low Out of Specification (OOS) results for dissolution.
Published: June 29, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clonazepam Orally Disintegrating Tablets, USP, 0.125mg, Rx Only, 60 Tablets, Mfd. by: Sun Pharmaceutical Industries Ltd. Mumbai, India, Dist. by: Sun Pharmaceutical Industries In., Cranbury, NJ 08512, NDC 57664-783-68, packaged in bottles.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Tablet/Capsule Specification; oversized tablet found in a bottle
Published: June 29, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate Injection, USP, 200 mg/mL, 1 mL Single-dose vial per carton, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-015-40.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Lack of Assurance of Sterility: Manufacturing deviation which was reported due to a microbial excursion
Published: June 29, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate Injection, USP, 200 mg/mL, 1 mL Single-dose vial per carton, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-015-40.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: CGMP Deviations: lots made with same active pharmaceutical ingredient (API) as lots that were rejected due to manufacturing issues that could cause the product to be out of specification for impurities.
Published: June 29, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clonidine Transdermal System, USP 0.3 mg/day, 4 Patches (NDC 51862-455-01) per Carton (51862-455-04), Rx only, Manufactured for: Mayne Pharma Greenville, NC 27834

by Mayne Pharma Inc

Reason: Defective Delivery System: Out of specification for release liner removal force results at the 3-month CRT stability timepoint.
Published: June 29, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

70% ISOPROPYL ALCOHOL First aid antiseptic, 4 FL OZ (118 mL) bottle, Made in US with US and foreign components for Medline Industries, Inc., Mundelein, IL 60060 USA, NDC: 53329-798-04, UPC (01) 10888277362291.

by Vi-Jon, LLC

Reason: Defective Container: Product may leak when squeezed or when not in an upright position determined to be due to defects in the bottle neck finish and insufficient tightening.
Published: June 29, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EarthLab Inc

Product: Wise Woman Herbals Sleepytime Glycerite. Product is liquid a…
Reason: The microbial test result is found to be out of specification due to high yeast and mold counts.
Published: June 29, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EarthLab Inc

Product: Wise Woman Herbals Standardized Kava Glycerite, product is l…
Reason: The microbial test result is found to be out of specification due to high yeast and mold counts.
Published: June 29, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EarthLab Inc

Product: Wise Woman Herbals Kava Capsules, 450 mg Kava (Piper met. Ro…
Reason: The microbial test result is found to be out of specification due to high yeast and mold counts.
Published: June 29, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Casper's Ice Cream, Inc

Product: Red Button Vintage Creamery Canadian Vanilla Ice Cream, 56 o…
Reason: Burnt Almond Fudge ice cream was packaged into Canadian Vanilla tubs during the run of the Burnt Almond Fudge. The Canadian Vanilla tubs do not list tree nut (almond) allergen in the ingredients list or contains statement leading to undeclared allergens.
Published: June 29, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product: Pedialyte with Immune Support***+Zinc/Selenium & Magnesium**…
Reason: These products are being recalled due to the potential of leakage from the 1L container.
Published: June 29, 2022
Distribution: AL, AR, AZ, CA, CO, DE, FL, GA, IA, IL,…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product: Pedialyte with Immune Support***+Zinc/Selenium & Magnesium**…
Reason: These products are being recalled due to the potential of leakage from the 1L container.
Published: June 29, 2022
Distribution: AL, AR, AZ, CA, CO, DE, FL, GA, IA, IL,…

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FDA Recall United States Terminated Historical recordClass I

Calico Cottage Inc

Product: 1. SALTED NUT ROLL PRE-MADE FUDGE (6SS) 6LB NET WT - not con…
Reason: Fudge contains peanut butter that is potentially contaminated with Salmonella.
Published: June 29, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Calico Cottage Inc

Product: 1. PEANUTTIEST CARAMEL CHOCOLATE P-MADE(6SS)6LB NT WT - not…
Reason: Fudge contains peanut butter that is potentially contaminated with Salmonella.
Published: June 29, 2022
Distribution: Nationwide

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Data last updated: September 15, 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.