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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.

37,060
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/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 921–940 of 19,170 recalls

FDA Recall Ongoing Historical recordClass II

Wecare Enema, 4.5 Fl Oz/133mL, Manufactured for: Dynarex Corporation, 11 Dynarex Corporation, MIddletown, NY 10941 USA, Made in India, NDC 67777-402-01.

by Blossom Pharmaceuticals

Reason
cGMP deviations
Published
December 10, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Dynashield Skin Protectant, Net Wt. 16 oz (453.6 g), Manufactured for: Dyrnarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962, USA, Made in India, NDC 67777-407-04.

by Blossom Pharmaceuticals

Reason
cGMP deviations
Published
December 10, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Lanashield Skin Barrier, 4 oz. (113 g), Manfuactured for: Dynarex Corporation, 10 Gleshaw Street, Orangeburg, NY 10962 USA, Made in India, UPC 616784126319.

by Blossom Pharmaceuticals

Reason
cGMP deviations
Published
December 10, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Bisoprolol Fumarate and Hydrochlorothiazide Tablets, USP, 2.5 mg/6.25 mg, packaged as (a) 30-count bottles, NDC-68462-878-30; (b) 100-count bottle, NDC-68462-878-01; (c) 500-count bottles, NDC-68462-878-05; Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, Inda. Manufactured for: Glenmark Pharmaceuticals, Inc., USA, Mahwah, NJ 07430.

by Glenmark Pharmaceuticals Inc., USA

Reason
Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe
Published
December 10, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Carton label: Testosterone Gel 1%, 2.5 grams per unit dose, CIII, 30 unit-dose packets, Rx only, Manufactured by: Actavis Laboratories, Inc, Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, NDC 0591-3216-30. Packet label: Testosterone Gel 1%, contains 2.5 grams, For topical use only, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054,NDC: 0591-3216-17.

by Teva Pharmaceuticals USA, Inc

Reason
Defective Container - A defect in the side-seal which allows leakage of product.
Published
December 10, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Phytonadione Injectable Emulsion, USP 10mg/mL, 10x1 mL Single-Dose Vial/carton, Rx Only, Mfd. by: Cipla Ltd. India At M/s Immacule Lifesciences PVT. Ltd. India. Mfd. for: Cipla USA, Inc. Warren, NJ 07059. Vial NDC# 69097-708-31; Carton NDC 69097-708-96

by Cipla Limited

Reason
Failed Stability Specifications: Observed OOS results: eg results for colour index
Published
December 10, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Food Club Finely Shredded Pizza Style Four Cheese Blend (con…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Completed Historical recordClass I

Genepro Protein, Inc.

Product
Genepro Whey 4th Generation Plasma Treated Protein, unflavor…
Reason
Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen
Published
December 10, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Prime Food Processing LLC.

Product
Lava Bun with Salted Egg Yolk orange packaging (Frozen) U…
Reason
Products do not declare milk in the Contains statement or the ingredient statement.
Published
December 10, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Prime Food Processing LLC.

Product
Lava Bun with Green Tea Flavor bright lime green packaging…
Reason
Products do not declare milk in the Contains statement or the ingredient statement.
Published
December 10, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Blonde Beard's

Product
Blonde Beard's Dojo Asian Wing Sauce, wing sauce hot sauce c…
Reason
Undeclared Soy
Published
December 10, 2025
Distribution
Product was distributed to Canada and th…

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Good & Gather Mozzarella & Parmesan shredded cheese blend, F…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Mozzarella and provolone shredded cheese blend (containing l…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Pizza style shredded cheese blend (containing low-moisture p…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Italian style shredded cheese blend (containing low-moisture…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Happy Farms by Aldi Italian Style shredded cheese blend (con…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Low-moisture part-skim mozzarella shredded cheese, individua…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Water Pure, Inc.

Product
My Bladder; Supports normal bladder tone & control; Dietary…
Reason
Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303
Published
December 10, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL vials, Rx only, Fresenius Kabi USA, LLC, NDC 63323-739-11 (unit of use), 63323-739-12 (unit of sale).

by Fresenius Kabi USA, LLC

Reason
Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
Published
December 3, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, NDC 0363-3114-01

by Medical Products Laboratories, Inc.

Reason
Microbial contamination of a non-sterile product - microorganism found to be pseudomonas lactis
Published
December 3, 2025
Distribution
Nationwide

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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.