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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

State: IL ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 25, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass I

Hy-Vee Stores Inc

Product: HyVee brand Pumpkin-flavored Bettercreme cheese cakes packag…
Reason: Product contained an ingredient that tested positive for Salmonella.
Published: February 13, 2019
Distribution: Distributed to consumers in Iowa, Illino…

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FDA Recall United States Terminated Historical recordClass I

Hy-Vee Stores Inc

Product: HyVee brand Golden Oreo-flavored cheese cakes packaged in th…
Reason: Product contained an ingredient that tested positive for Salmonella.
Published: February 13, 2019
Distribution: Distributed to consumers in Iowa, Illino…

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FDA Recall United States Terminated Historical recordClass I

Hy-Vee Stores Inc

Product: HyVee brand Smores-flavored Bettercreme cheese cakes package…
Reason: Product contained an ingredient that tested positive for Salmonella.
Published: February 13, 2019
Distribution: Distributed to consumers in Iowa, Illino…

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FDA Recall United States Terminated Historical recordClass I

Hy-Vee Stores Inc

Product: HyVee brand Pumpkin-fluff -flavored cheese cakes packaged in…
Reason: Product contained an ingredient that tested positive for Salmonella.
Published: February 13, 2019
Distribution: Distributed to consumers in Iowa, Illino…

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FDA Recall United States Terminated Historical recordClass I

Hy-Vee Stores Inc

Product: HyVee brand Oreo-flavored cheese cakes packaged in the follo…
Reason: Product contained an ingredient that tested positive for Salmonella.
Published: February 13, 2019
Distribution: Distributed to consumers in Iowa, Illino…

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FDA Recall United States Terminated Historical recordClass I

Funky Chunky LLC

Product: Nutty Choco Pop, 10 oz. bag. Sold in the following configur…
Reason: Nutty Choco Pop has in incorrect label and does not declare that it contains cashews and almonds.
Published: February 13, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Pizza Blends, LLC

Product: The Great American by Pizza Blends, Pizza Dough Mix With Yea…
Reason: The firm received an ingredient from their supplier that is potentially contaminated with Salmonella.
Published: February 13, 2019
Distribution: Distributed to customers in AR, CO, FL,…

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FDA Recall Terminated Historical recordClass II

Fexofenadine HCl Tablets, USP, 180 mg, packaged in a) 30-count bottles (NDC 0378-0782-93) and b) 500-count bottles (NDC 0378-0782-05); Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA.

by Mylan Pharmaceuticals Inc.

Reason: Failed Impurities/Degradation Specifications: Related compound results obtained during routine stability testing was slightly elevated above specification.
Published: February 6, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BromSite (bromfenac ophthalmic solution) 0.075%, 5 mL bottles, Rx Only, Distributed by : Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, NDC 49708-754-41

by Sun Pharmaceutical Industries, Inc.

Reason: Bromfenac Ophthalmic Solution, 0.075% (Sterile 5 mL) may have a lack of sterility assurance.
Published: February 6, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

GENTAMICIN OPTH-SOL 5ml Compare: Garamycin. 5-mL plastic dropper bottle, Mfg: AKORN 17478-0283-10. NDC 52959-0103-00

by H J Harkins Company Inc dba Pharma Pac

Reason: Presence of Particulate Matter: Crystalline particles were noticed by manufacturer at the 24 month clarity testing.
Published: February 6, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Gentamicin Sulfate Ophthalmic Solution, USP 0.3%, 5 mL dropper bottle, Rx Only, Manufactured by: Akorn, Inc. Lake Forest, IL 60045, NDC 17478-283-10

by Akorn, Inc.

Reason: Presence of Particulate Matter: Crystalline particles were noticed at the 24 month clarity testing.
Published: February 6, 2019
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Irbesartan and Hydrochlorothiazide Tablets, USP 150/12.5 mg Rx 30 Tablets Only Manufactured by: Zhejiang Huahai Pharmaceutical Co., Ltd. Xunqiao, Linhai, Zheijang 317024, China Distributed by: Solco Healthcare US, LLC Cranbury, NJ 08512 NDC 43547-330-03

by Prinston Pharmaceutical Inc

Reason: CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodimethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of 0.083 parts per million.
Published: February 6, 2019
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Irbesartan and Hydrochlorothiazide Tablets, USP 300/12.5 mg Rx Only Manufactured by: Zhejiang Huahai Pharmaceutical Co., Ltd. Xunqiao, Linhai, Zheijang 317024, China Distributed by: Solco Healthcare US, LLC Cranbury, NJ 08512 90 count NDC 43547-331-09

by Prinston Pharmaceutical Inc

Reason: CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodimethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of 0.083 parts per million.
Published: February 6, 2019
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Irbesartan and Hydrochlorothiazide Tablets, USP 300/12.5 mg Rx Only Manufactured by: Zhejiang Huahai Pharmaceutical Co., Ltd. Xunqiao, Linhai, Zheijang 317024, China Distributed by: Solco Healthcare US, LLC Cranbury, NJ 08512 30 count - NDC 43547-331-03

by Prinston Pharmaceutical Inc

Reason: CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodimethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of 0.083 parts per million.
Published: February 6, 2019
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Irbesartan and HydrochlorothiazideTablets, USP 150/12.5 mg Rx Only 90 count Manufactured by: Zhejiang Huahai Pharmaceutical Co., Xunqiao, Linhai, Zhejiang 317024 China Distributed by: Solco Healthcare US, LLC Cranbury, NJ 08512 NDC 43547-330-09

by Prinston Pharmaceutical Inc

Reason: CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodimethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of 0.083 parts per million.
Published: February 6, 2019
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Irbesartan Tablets 300 mg 90 count Rx only Manufactured by: Zhejiang Huahai Pharmaceutical Co., Xunqiao, Linhai, Zhejiang 317024 China Distributed by: Solco Healthcare US, LLC Cranbury, NJ 08512 NDC 43547-376-09

by Prinston Pharmaceutical Inc

Reason: CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodimethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of 0.083 parts per million.
Published: February 6, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Jac Vandenberg Inc.

Product: Plums sold at ALDI, packaged in a 2-pound bag with the brand…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: February 6, 2019
Distribution: Alabama, California, Georgia, Illinois,…

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FDA Recall United States Terminated Historical recordClass I

Jac Vandenberg Inc.

Product: Nectarines sold as a bulk retail item, with PLU 3035 (white…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: February 6, 2019
Distribution: Alabama, California, Georgia, Illinois,…

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FDA Recall United States Terminated Historical recordClass I

Jac Vandenberg Inc.

Product: Peaches, sold as a bulk retail item, with PLU 4044, and coun…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: February 6, 2019
Distribution: Alabama, California, Georgia, Illinois,…

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FDA Recall Terminated Historical recordClass II

Fluocinolone Acetonide Topical Solution, USP, 0.01 %, 60 mL bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202; Manufactured by: Novel Laboratories, Inc., Somerset, NJ 08873; NDC 43386-069-60.

by LUPIN SOMERSET

Reason: Failed Impurities/Degradation Specifications: Expansion of October 2018 recall due to elevated out of specification results for total impurities that have been chemically identified as oxidative degradation products of the fluocinolone active pharmaceutical ingredient.
Published: January 30, 2019
Distribution: Nationwide

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Data last updated: September 25, 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.