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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: ND ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 16, 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 Terminated Historical recordClass II

Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%) 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0071-5, UPC 851722007125

by Eosera, Inc.

Reason: cGMP Deviations.
Published: August 19, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ear Pain MD Pain Relief Drops with 4% Lidocaine (lidocaine HCl Monohydrate 4%) 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0072-2

by Eosera, Inc.

Reason: cGMP Deviations.
Published: August 19, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ear Pain MD Pain Relief Drops For Kids (lidocaine HCl Monohydrate 4%) 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0070-8

by Eosera, Inc.

Reason: cGMP Deviations.
Published: August 19, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clobetasol Propionate Cream, USP, 0.05%, packaged in a)15g Tubes (NDC 60429-902-15) and b) 45g Tubes (NDC 60429-902-45), Rx Only, Mfd. by: Taro Pharmaceuticals Inc. Brampton, Ontario, Canada, Marketed by: Golden State Medical Supply Inc. Camarillo, CA 93012.

by Golden State Medical Supply Inc.

Reason: Failed Content Uniformity: bulk lot used to make these two lots was found to have failed content uniformity.
Published: August 19, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clobetasol Propionate Cream USP, 0.05%, a) 15 g tube, NDC: 60429-902-15; b) 45 g tube, NDC: 60429-902-45, Rx Only, For External Use Only, Not for Ophthalmic Use, Mfd by: Taro Pharmaceuticals Inc. Brampton, Ontario, Canada L6T 1C1, Marketed by: Golden State Medical Supply, Inc. Camarillo, CA 93012.

by Taro Pharmaceuticals U.S.A., Inc.

Reason: Failed Content Uniformity: bulk lot used to make these two lots was found to have failed content uniformity.
Published: August 19, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Heparin Sodium 5,000 units in 0.9% Sodium Chloride 1000 mL bag (5 units/mL), Rx only, SCA Pharmaceuticals 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0650-46

by SCA Pharmaceuticals

Reason: Subpotent Drug: Out-of-Specification potency results at the 30-day stability timepoint.
Published: August 19, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Nystatin Oral Suspension, USP 100,000 units per mL, Cherry/Peppermint Flavor, 16 fl. oz. (473 mL), Rx only, Pharmaceutical Associates, Inc. Greenville, SC 29605, NDC 0121-0810-16

by PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Reason: Subpotent drug: Out of specification for assay at the 15-month test interval.
Published: August 19, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lidocaine Patch 5%, packaged in 30-count cartons, Rx only, Manufactured by: Actavis Laboratories UT, Inc., Salt Lake City, UT 84108, USA, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054 USA, NDC 0591-3525-30

by Teva Pharmaceuticals USA

Reason: Labeling: Incorrect or Missing Lot and/or Exp date on the individual transdermal pouches but not in the carton.
Published: August 19, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Hostess Brands, LLC

Product: Hostess Raspberry Zingers, Raspberry Iced Cake With Creamy F…
Reason: Product potentially has mold prior to best by date.
Published: August 19, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Upspring,ltd

Product: UpSpring Baby Iron + Immunity MULTI + IRON + ZINC Promotes n…
Reason: May contain undeclared milk
Published: August 19, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Wellements LLC

Product: Iron Drops Sampler (UPC 729609000098) liquid Dietary Supplem…
Reason: Product contains undeclared milk
Published: August 19, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Wellements LLC

Product: Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 o…
Reason: Product contains undeclared milk
Published: August 19, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1% - antimicrobial), For Institutional and Industrial Use Only, a) foamyiQ 42.27 oz/1250 mL cartridge, UPC code: 7 53727 26454 4; b) Lite 'n Foamy 1 gallon/3.79 L container UPC code: 7 53727 26113 0, Spartan Chemical Company, Inc., 1110 Spartan Drive, Maumee, OH 43537 USA.

by Spartan Chemical Co Inc

Reason: Microbial contamination of non-sterile products: positive microbial contamination in product.
Published: August 12, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

VILEVEV MB Urinary Antispetic (81.0 mg methenamine, 40.8 mg sodium phosphate monobasic and 10.8 mg methylene blue, 0.12 mg hyoscyamine sulfate and 32.4 mg phenyl salicylate), Rx Only, 90 Tablets per Bottle, Manufactured for: Vilvet Pharmaceuticals, Inc., Chester Springs, PA 19425, NDC 71186-000-24.

by Vilvet Pharmaceuticals Inc.

Reason: cGMP deviations
Published: August 12, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

VILAMIT MB (118 mg methenamine, 36 mg phenyl salicylate, 40.8 mg sodium phosphate monobasic, 10.0 mg methylene blue and 0.12 mg hyoscyamine sulfate), Rx Only, 100 Capsules per Bottle, Manufactured for: Vilvet Pharmaceuticals Inc., Chester Springs, PA 18425, NDC 71186-002-35.

by Vilvet Pharmaceuticals Inc.

Reason: cGMP deviations
Published: August 12, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Tropical Lip Moisturizer, SPF 30, UVA/UVB Lip Protection, Active Ingredients: Oxybenzone 5%, Octisalate 5%, Octinoxate 7.5%, Meradimate 5%, Made in USA

by Yusef Manufacturing Laboratories, LLC

Reason: Superpotent Drug: The beginning portion of the batch appears to be approximately 25% superpotent for active ingredient Meradimate.
Published: August 12, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Daptomycin for Injection, 500 mg/vial, Single-Dose Vial, Rx only, Sterile, Manufactured for: Mylan Institutional, LLC, Rockford, IL 61103 USA, NDC 67457-813-50

by Mylan Institutional LLC

Reason: Presence of Particulate Matter
Published: August 12, 2020
Distribution: Nationwide

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FDA Recall Completed Historical recordClass I

Herbzeedy, Hemp Oil Full Spectrum, Natural, 1500 MG CBD, 1 FL OZ (30 ML) bottles, Distributed by: Herbzeedy, Statesboro, GA

by MICHIGAN HERBAL REMEDIES

Reason: Chemical contamination: product contains elevated levels of undeclared lead.
Published: August 12, 2020
Distribution: Nationwide

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FDA Recall Completed Historical recordClass I

Goodness Gurus, Healthy Hemp Drops, 1500 MG/Spearmint, 1 FL. OZ bottles, Distributed by: Goodness Gurus, Inc., Carlisle, PA, UPC 6 53341 99411 0

by MICHIGAN HERBAL REMEDIES

Reason: Chemical contamination: product contains elevated levels of undeclared lead.
Published: August 12, 2020
Distribution: Nationwide

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FDA Recall Completed Historical recordClass I

Goodness Gurus, Healthy Hemp Drops Full Strength, 1000 MG/Spearmint, 1 FL. OZ bottles, Distributed by: Goodness Gurus, Inc., Carlisle, PA, UPC 53341 99311 3

by MICHIGAN HERBAL REMEDIES

Reason: Chemical contamination: product contains elevated levels of undeclared lead.
Published: August 12, 2020
Distribution: Nationwide

View recall →

Data last updated: September 16, 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.