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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,139
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026
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)

  • 1,527 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

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

Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 12,001–12,020 of 17,335 recalls

FDA Recall United States Terminated Historical recordClass II

Bio-Botanica, Inc.

Product
Liquid VITAMIN D-3 Drops distributed under the following pri…
Reason
The lots exceed the label claim for Vitamin D3 of 2000 IU per drop.
Published
January 4, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Cargill Cocoa & Chocolate, Inc.

Product
Wilbur; IM10021; B558 Semisweet Chocolate Drops, 2000 CT; Ne…
Reason
Cargill Cocoa & Chocolate is recalling 50 lb. cartons of Wilbur B558 Semi-Sweet Chocolate Drops because it may contain undeclared milk.
Published
January 4, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

COMFORT SHIELD (dimethicone) Barrier Cream Cloths, 3%, packaged as impregnated cloths wrapped in flexible packaging, further packed into inner cartons, with the inner cartons are placed into an over shipper sold in a) 3-count disposable barrier cloths per package, 45 packages per carton, 2 cartons (90 packages) per case, Reorder # 7503, NDC 53462-915-50; b) 8-count disposable barrier cloths per package, 24 packages per carton, 2 cartons (48 packages) per case, Reorder # 7905, NDC 53462-915-80; c) 3-count disposable barrier cloths per package, 50 packages per carton, 2 cartons (100 packages) per case, Reorder # 7502, NDC 53462-915-51; d) 8-count disposable barrier cloths per package, 24 packages per carton, 2 cartons (48 packages) per case, Reorder # 7508, NDC 53462-915-81; e) 24-count disposable barrier cloths per tub, 12 packages per case, Reorder # 7524, NDC 53462-915-60; f) 24-count disposable barrier cloths per package, 9 packages per carton, 2 cartons (18 packages) per case, Reorder # 7526, NDC 53462-0915-62; Sage Products LLC, 3909 Three Oaks Road, Cary, Illinois 60013.

by Sage Products LLC

Reason
CGMP Deviations: potential contamination of products manufactured on the same equipment and lines as the contaminated product.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

BLACK LABEL X capsules, 60-count bottles, Manufactured for: Making it A Lifestyle, L.L.C.

by Making It a Lifestyle

Reason
Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Bupivacaine Hydrochloride Inj., USP (2.5 mg/mL) 0.25%, packaged in 30 mL Single-dose Preservative-Free vials, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1159-02

by Hospira Inc., A Pfizer Company

Reason
Presence of particulate matter: Confirmed customer report for the presence of particulate matter within a single vial.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Hyoscyamine Sulfate, USP Tablets, 0.125 mg, 100-count tablets per bottle, Rx only, Manufactured for: Virtus Pharmaceuticals OPCO II, LLC., Nashville, TN 37217, NDC 76439-308-10.

by VIRTUS PHARMACEUTICALS OPCO II L

Reason
Failed Content Uniformity Specifications: resulting in both superpotent and subpotent tablets.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Hyoscyamine Sulfate, Sublingual Tablets, 0.125 mg, 100-count bottle, Rx only, Manufactured for: Virtus Pharmaceuticals OPCO II, LLC., Nashville, TN 37217, NDC 76439-309-10.

by VIRTUS PHARMACEUTICALS OPCO II L

Reason
Failed Content Uniformity Specifications: resulting in both superpotent and subpotent tablets.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

2% Chlorhexidine Gluconate* Cloth, 2 disposable cloths per package, further packaged into 96 packages per case, labeled as a) Reorder #9705, b) Reorder #9701-P, and c) Reorder #9780, Sage Products LLC 3909 Three Oaks Road, Cary, Illinois 60013, NDC 53462-705-20.

by Sage Products LLC

Reason
CGMP Deviations: potential contamination of products manufactured on the same equipment and lines as the contaminated product.
Published
December 28, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

COMFORT SHIELD (dimethicone) Barrier Cream Cloths, 3%, packaged as impregnated cloths wrapped in flexible packaging, further packed into inner cartons, with the inner cartons are placed into an over shipper sold in a) 3-count disposable barrier cloths per package, 45 packages per carton, 2 cartons (90 packages) per case, Reorder # 7503, NDC 53462-915-50; b) 8-count disposable barrier cloths per package, 24 packages per carton, 2 cartons (48 packages) per case, Reorder # 7905, NDC 53462-915-80; c) 24-count disposable barrier cloths per package, 9 packages per carton, 2 cartons (18 packages) per case, Reorder # 7526, NDC 53462-0915-62; Sage Products LLC, 3909 Three Oaks Road, Cary, Illinois 60013.

by Sage Products LLC

Reason
Microbial Contamination of Non-Sterile Products: contamination with the bacteria, Burkholderia cepacia.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick, Distributed by: Tom's of Maine, Kennebunk, ME 04043, Made in Canada, Unit UPC: 077326831953 Case UPC: 10077326831950

by Les Emballages Knowlton Inc.

Reason
Labeling: Label Mix Up- Incorrect back label applied to the product.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Skinny Bee Diet capsules, 500 mg, packaged in a 60-count bottle

by Love My Tru Body

Reason
Marketed without an approved NDA/ANDA: presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and phenolphthalein.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

3rd DEGREE capsules, 60-count bottles, Manufactured for: Making it A Lifestyle, L.L.C.

by Making It a Lifestyle

Reason
Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

BLACK GOLD X ADVANCED capsules, 60-count bottles, Manufactured for: Making it A Lifestyle, L.L.C.

by Making It a Lifestyle

Reason
Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

GlucaGen HypoKit (glucagon [rDNA origin] for injection), 1 mg per vial, Single use only, Rx Only, Manufactured by: Novo Nordisk A/S 2880 Bagsvaerd, Denmark, NDC 0169-7065-15

by Novo Nordisk Inc

Reason
Defective delivery system: detached needles on the syringe in the kit.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Honeywell eyesaline Eyewash Sterile Isotonic Solution, sterile water 99%, 32 fl. oz. (946 ml.), Sperian Eye & Face Protection, Inc. (a Honeywell Company), Platteville, WI 53818

by Sperian Eye & Face Protection, Inc

Reason
Non Sterility; contaminated with Klebsiella pneumoniae
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Lamotrigine Orally Disintegrating Tablets (ODT), 200 mg, 30 Tablets 3 blisters containing 10 tablets each, Rx only, Manufactured by: Watson Pharma Private Ltd., Verna, Salcette Goa INDIA, Distributed by: Impax Generics, Hayward, CA

by Impax Laboratories, Inc.

Reason
Labeling; Label Mixup; box labeled to contain 200 mg blister packs but actually contain 100 mg blister packs
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Hyoscyamine Sulfate, Orally Disintegrating Tablets, 0.125 mg, 100-count bottles, Rx only, Manufactured for: Virtus Pharmaceuticals OPCO II, LLC., Nashville, TN 37217, NDC 76439-307-10.

by VIRTUS PHARMACEUTICALS OPCO II L

Reason
Failed Content Uniformity Specifications: resulting in both superpotent and subpotent tablets.
Published
December 28, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Ultimate Body Tox PRO capsules, Proprietary Blend, 350 mg, 45 count bottle, Manufactured for: JSN Health, 305 Broadway, 7th Floor, New York, NY 10007.

by Ultimate Body Tox

Reason
Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine. The presence of sibutramine, a previously approved controlled substance that was removed from the U.S. market in October 2010 for safety reasons, in this tainted product renders it an unapproved drug for which safety and efficacy have not been established and therefore subject to recall.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

BuPROPion Hydrochloride Extended-Release Tablets (XL), 300 mg, Rx Only, a) 30 count bottles (NDC 68382-354-06) and b) 500 count bottles (NDC 68382-354-05), Manufactured by: Cadila Healthcare LTD. Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534

by Zydus Pharmaceuticals USA Inc

Reason
Failed Dissolution Specifications; 6 month time point
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Simply Fresh Fruit

Product
3 GL PAIL SFF SEASONAL FRUIT MIX B, UPC 4294710277
Reason
Simply Fresh Fruit is recalling cantaloupe and fruit mixes with cantaloupe because they may be contaminated with Listeria monocytogenes.
Published
December 28, 2016
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.