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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

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

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Source: FDA and USDA public dataLast updated September 13, 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 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 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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FDA Recall United States Terminated Historical recordClass I

Calico Cottage Inc

Product: 1. PEANUT BUTTER FUDGE (3 - 6LB SLABS/CS) 18LB NET WT - not…
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. PEANUT BUTTER CHOC (3 - 6LB SLABS/CS) 18LB NET WT - Not c…
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

Albanese Confectionery Group, Inc.

Product: Rich s Milk Chocolate Giant Layered Peanut Butter and Cups R…
Reason: Salmonella. Product made using recalled Jif peanut butter
Published: June 29, 2022
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, a) 100-count bottles labeled with UPC 7 501031 111190 and UPC 6 09002 40885, and b) 2 pack of 100-count bottles per carton UPC 3 72426 01434

by Walmart Inc

Reason: Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
Published: June 22, 2022
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.

by Walmart Inc

Reason: Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
Published: June 22, 2022
Distribution: Nationwide

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FDA Recall Completed Historical recordClass I

Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800, Mexico, D.F., UPC 7 501031 111190.

by Walmart Inc

Reason: Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.
Published: June 22, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Zileuton Extended-Release Tablets, 600 mg, 120-count bottle, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD 21202 by Lupin Limited, Nagpur-441108, India, NDC 68180-169-16

by Lupin Pharmaceuticals Inc.

Reason: Failed Dissolution Specifications: Out of specification test results observed in dissolution testing during long term stability study.
Published: June 22, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Premium Nature Instant Hand Sanitizer, (ethyl alcohol 65%), 8 oz/ 236 ML plastic bottles; Premium Nature, South Plainfield, NJ. UPC 819192028668

by AMS Packaging Inc

Reason: Subpotent Drug: FDA analysis has revealed some bottles of these products were sub potent for ethanol.
Published: June 22, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

medroxyPROGESTERone Acetate Injectable Suspension, USP, 25 x 1 mL Single-Dose Vial, 150 mg/mL, 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 16714-090-40 packaged in 25 count carton.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Lack of assurance of sterility
Published: June 22, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Single-Dose Vial, 150 mg/mL, Rx only, Manufactured for: Northstart Rx LLC, Memphis, TN, 38141, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol Baroda Highway, Halol-389 350, Gujarat India , NDC 16714-981-01.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Lack of assurance of sterility
Published: June 22, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured by Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 62756-091-40.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Lack of assurance of sterility
Published: June 22, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 16714-999-01.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Lack of assurance of sterility
Published: June 22, 2022
Distribution: Nationwide

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Data last updated: September 13, 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.