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Recall totals

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

37,327
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,859
Class I recallsReasonable probability of serious health consequences
24,440
Class II recallsTemporary or medically reversible health consequences
2,900
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 2,095 recalls
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 2026 is incomplete and not included in the figures above.
  • Complete data
  • Incomplete
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,440
Class I9,859
Class III2,900
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,440
Class I9,859
Class III2,900
Not Yet Classified2

Showing 6,501–6,520 of 17,449 recalls

FDA Recall TerminatedTerminated: December 10, 2020Historical 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

View recall →

FDA Recall TerminatedTerminated: June 20, 2023Historical 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

View recall →

FDA Recall TerminatedTerminated: March 17, 2021Historical 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 TerminatedTerminated: September 22, 2021Historical 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 TerminatedTerminated: July 7, 2021Historical 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 TerminatedTerminated: January 11, 2021Historical 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 TerminatedTerminated: June 3, 2021Historical 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 TerminatedTerminated: January 22, 2021Historical 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 TerminatedTerminated: January 22, 2021Historical 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

View recall →

FDA Recall TerminatedTerminated: October 16, 2023Historical 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 TerminatedTerminated: January 21, 2022Historical 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 TerminatedTerminated: January 21, 2022Historical 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

View recall →

FDA Recall TerminatedTerminated: February 13, 2024Historical 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 TerminatedTerminated: January 27, 2023Historical 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 CompletedHistorical 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 CompletedHistorical 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

View recall →

FDA Recall CompletedHistorical 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 →

FDA Recall CompletedHistorical recordClass I

BC Hemp Co., Full Spectrum Hemp Extract, CBD Oil, Natural, 1000MG CBD, 1 FL. OZ (30 ML) bottles, Distributed by: B.C. Hemp Co., LLC, P.O. Box 156, Eau Claire, MI 49111

by MICHIGAN HERBAL REMEDIES

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

View recall →

FDA Recall CompletedHistorical recordClass I

BC Hemp Co., Full Spectrum Hemp Extract, CBD Oil , Berry Blast, 1000MG CBD, 1 FL. OZ (30ML) bottles, Distributed by: B.C. Hemp Co., LLC, P.O. Box 156, Eau Claire, MI 49111

by MICHIGAN HERBAL REMEDIES

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

View recall →

FDA Recall CompletedHistorical recordClass I

Tasty Drops, Hemp Oil Extract, Vanilla, 500MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29082 8

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:

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.

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