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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.

37,066
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

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 3,181–3,200 of 18,528 recalls

FDA Recall Terminated Historical recordClass II

Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 15-count cartons, Distributed By: Adusa Distribution, LLC, Salisbury, NC 28147. NDC 72476-847-22

by L. Perrigo Company

Reason
Failed Impurities/Degradation Specifications
Published
July 19, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Non-Drowsy Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 150-count cartons, Distributed By: BJ's Wholesale Club, 25 Research Drive, Westborough, MA 01581. NDC 68391-847-47

by L. Perrigo Company

Reason
Failed Impurities/Degradation Specifications
Published
July 19, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Allergy, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 72288-847-39), and b)150-count cartons (NDC 72288-847-47 and 72288-847-37), Distributed By: Amazon.com Services LLC., 410 Terry Avenue N., Seattle, WA 98109.

by L. Perrigo Company

Reason
Failed Impurities/Degradation Specifications
Published
July 19, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Dry Eye Relief Lubricant Eye Drops, (Glycerin 0.2%, Hypromellose 0.2 %, Polyethylene glycol 400 1%), 0.5 FL OZ (15mL) bottle, packaged in a) equate, DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716, 2-0.5 FL OZ (15 mL) Bottles, 1 FL OZ (30 mL) TOTAL, UPC 6 81131 36701 1, NDC 49035-280-02; b) DG health, DISTRIBUTED BY OLD EAST MAIN CO., 100 MISSION RIDGE, GOODLETTSVILLE, TN 37072, UPC 0 95072 02656 0; c) sunmark, Distributed By McKesson, 6555 State Highway 161, Irving, TX 75039, UPC 0 10939 62144 3, NDC 49348-037-29; d) TopCare health, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007, UPC 0 36800 36100 3; e) HealthMart, Distributed by McKesson, 6555 State Highway 161, Irving, TX 75039, UPC 0 52569 13715 4; f) exchange select Artificial Tears, Manufactured for your Military Exchanges by: KC Pharmaceuticals, Inc., Pomona, CA 91768, UPC 6 14299 05620 6; g) meijer, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544, UPC 7 13733 29692 2, NDC 41250-718-01; h) H.E.B, MADE WITH PRIDE AND CARE FOR H.E.B, SAN ANTONIO, TX 78204, UPC 0 41220 43741 2; i) GeriCare, Distributed by: Gericare Pharmaceuticals Corp., 1650 63rd St., Brooklyn, NY 11204, UPC 3 57896 18405 6, NDC 57896-181-05

by K.C. Pharmaceuticals, Inc

Reason
CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.
Published
July 19, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Original Eye Drops; Redness Reliever; (Tetrahydrozoline HCl), 0.05%, 0.5 FL OZ (15mL); distributed by a) Original Formula Eye Drops, DG health, DISTRIBUTED BY OLD EAST MAIN CO, 100 MISSION RIDGE, GOODLETTSVILLE, TN 37072, UPC 0 95072 00556 5; b) Publix, DISTRIBUTED BY PUBLIX SUPER MARKETS, INC, 3300 PUBLIX CORPORATE PARKWAY, LAKELAND, FL 33811, UPC 0 41415 01076 5; c) sterile eye drops, Original Formula, sunmark, Distributed by McKesson, 6555 State Highway 161, Irving, TX 75039, UPC 0 10939 16733 0, NDC 49348-037-29; d) TopCare health, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELKGROVE VILLAGE, IL 60007, UPC 0 36800 03639 0; e) Eye Drops, Original Formula, GoodSense, Distributed By: Geiss, Destin & Dunn, Inc., Peachtree City, GA 30269, UPC 1 80410 00015 6, NDC 50804-141-01; f) sterile eye drops, Circle K, Product manufactured for: Lil' Drug Store Products, Inc., 9300 Earhart Lane SW, Cedar Rapids, IA 52404 Proudly distributed by Circle K Stores Inc., UPC 1 94283 65185 8; g) Sterile Eye Drops, Regular Formula, Lil Drug Store, Product manufactured for: Lil' Drug Store Products, Inc., 9300 Earhart Lane SW, Cedar Rapids, IA 52404; UPC 3 66715 68324 3; h) Tetrahydrozoline Ophthalmic Solution, Rugby, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, UPC 3 05361 21794 5, NDC 0536-1217-94, i) Leader, DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, UPC 0 96295 13645 6, NDC 70000-0454-1; j) REDNESS RELIEF EYE DROPS, CAREone, Distributed by: FOODHOLD USA, LLC, LANDOVER, MD 20785; UPC 0 41520 86531 1, NDC 41520-431-05; k) Eye Drops, Original Formula, Good Neighbor Pharmacy, Distributed By AmerisourceBergen, 1300 Morris Drive, Chesterbrook, PA 19087, UPC 0 87701 14975 7, NDC 24385-075-05; l) Eye Drops, ORIGINAL FORMULA, Walgreens, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, UPC 3 11917 20076 7; m) CVS Health, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 36131 3; n) H-E-B, MADE WITH PRIDE & CARE FOR H-E-B, SAN ANTONIO, TX 78204, UPC 0 41220 43747 4; o) redness relief, Original Redness Reliever Eye Drops, meijer, DIST. BY MEIJER DISTRIBUTION INC., GRAND RAPIDS, MI 49544, UPC 0 41250 82916 4, NDC 41250-814-01; p) Eye Drops, ORIGINAL, Best Choice, PROUDLY DISTRIBUTED BY: VALU MERCHANDISERS, CO., 5000 KANSAS AVE, KANSAS CITY, KS 66106, UPC 0 70038 47011 3

by K.C. Pharmaceuticals, Inc

Reason
CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.
Published
July 19, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

PANCREAZE (pancrelipase) Delayed-Release Capsules, 100-count bottles, Rx only, Rx only, Manufactured by VIVUS LLC, Campbell, CA 95008, UPC: N3 62541-401-10 5, NDC 62541-401-10,

by Vivus, Inc.

Reason
Failed Stability Specifications
Published
July 19, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dakota Style, Inc

Product
Gelson's Sea Salt Pretzels, 4.5oz poly bags, UPC: 23631-1118…
Reason
May contain undeclared milk
Published
July 19, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dakota Style, Inc

Product
1. Hy-Vee Dill Pickle Braided Pretzels, 10oz poly bags, UPC:…
Reason
May contain undeclared milk
Published
July 19, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dakota Style, Inc

Product
1. Hy-Vee Honey Mustard Braided Pretzels, 10oz poly bags, UP…
Reason
May contain undeclared milk
Published
July 19, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dakota Style, Inc

Product
1. Hy-Vee Salt & Vinegar Braided Pretzels, 10 oz poly bags,…
Reason
May contain undeclared milk
Published
July 19, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Oregon Potato Company

Product
Rader Farms Organic Fresh Start Smoothie Blueberry, Strawber…
Reason
Potential contamination with Hepatitis A.
Published
July 19, 2023
Distribution
All products distributed in AR, AZ, CA,…

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FDA Recall United States Terminated Historical recordClass I

Oregon Potato Company

Product
Rader Farms Organic Berry Trio Strawberry, Blackberry, Raspb…
Reason
Potential contamination with Hepatitis A.
Published
July 19, 2023
Distribution
All products distributed in AR, AZ, CA,…

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FDA Recall United States Terminated Historical recordClass I

Oregon Potato Company

Product
Great Value Antioxidant Fruit Blend Strawberries, Blueberrie…
Reason
Potential contamination with Hepatitis A.
Published
July 19, 2023
Distribution
All products distributed in AR, AZ, CA,…

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FDA Recall United States Terminated Historical recordClass I

Oregon Potato Company

Product
Great Value Mixed Fruit Pineapple, Strawberries, Peaches and…
Reason
Potential contamination with Hepatitis A.
Published
July 19, 2023
Distribution
All products distributed in AR, AZ, CA,…

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FDA Recall United States Terminated Historical recordClass I

Oregon Potato Company

Product
Great Value Sliced Strawberries. Item # 107356. Frozen, pack…
Reason
Potential contamination with Hepatitis A.
Published
July 19, 2023
Distribution
All products distributed in AR, AZ, CA,…

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FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram- 603 110, Tamilnadu, India, NDC 64380-933-08

by Strides Pharma Inc.

Reason
Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.
Published
July 12, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Tizanidine Hydrochloride Tablet 4mg, packaged in a) 20 count-bottles (NDC 68788-7781-2), b)30-count bottles (NDC: 68788-7781-3), c) 60-count bottles, (NDC: 68788-7781-6), d) 90-count bottles (NDC: 68788-7781-9), e) 120-count bottles (NDC: 68788-7781-8), Rx only, Mfg: Dr. Reddy's Laboratories Limited.

by Preferred Pharmaceuticals, Inc.

Reason
Failed Stability Specifications
Published
July 12, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Tizanidine Tablets, USP, 4 mg, 100 Tablets (10 tablets x 10 unit dose blister packs) per carton, Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC 68084-645-01 (carton), barcode (01) 003 68084 645 11 2.

by Amerisource Health Services LLC

Reason
Failed Dissolution Specifications: this repackaged product was recalled by the manufacturer, Dr. Reddy's Laboratories, Inc., due to out of specification results for dissolution.
Published
July 12, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Supplement Manufacturing Partner, Inc.

Product
Havasu Beetroot Powder, 11.5 oz.
Reason
Contains undeclared milk
Published
July 12, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Avery Brewing Company

Product
Gose con Sandia, Sour Ale with watermelon, limes and sea sal…
Reason
Due to over pressurization, can may fail/explode.
Published
July 12, 2023
Distribution
Multiple states

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.