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Recall totals

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

37,135

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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 23, 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 II

Rich Products Corp

Product: VANILLA WHIPPED ICING ARTIFICALLY FLAVORED Product Number: 0…
Reason: Possible contamination with cleaning chemicals.
Published: December 12, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clindamycin Phosphate Topical Solution USP, 1% (10 mg/mL clindamycin), 60 pledget applicators per jar, Rx only. Manufactured by Ei LLC 2865 N. Cannon Blvd. Kannapolis, NC 18083. NDC# 61748-0201-60

by Akorn, Inc.

Reason: Failed Impurities/Degradation Specifications; out of specification results observed for other individual impurities
Published: December 5, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Quetiapine Tablets USP 400 mg, 100 tablet bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, India. Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 --- NDC 67877-248-01, UPC code: 3 67877-248-01 1

by Ascend Laboratories LLC

Reason: Presence of Foreign Substance; metal shard found in tablet
Published: December 5, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Chukar Cherry Company

Product: Organic Ultra Dark Orange Chocolate Tart Cherries, Chukar Ch…
Reason: Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Published: December 5, 2018
Distribution: Distributed in AK, AZ, CA, CO, MD, ME, M…

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FDA Recall United States Terminated Historical recordClass I

Chukar Cherry Company

Product: Organic Ultra Dark Vanilla Chocolate Rainier Cherries, Chuka…
Reason: Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Published: December 5, 2018
Distribution: Distributed in AK, AZ, CA, CO, MD, ME, M…

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FDA Recall United States Terminated Historical recordClass I

Chukar Cherry Company

Product: Ultra Dark Chocolate Cocoa Pecans, Chukar Cherries brand, pa…
Reason: Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Published: December 5, 2018
Distribution: Distributed in AK, AZ, CA, CO, MD, ME, M…

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FDA Recall United States Terminated Historical recordClass I

Chukar Cherry Company

Product: Ultra Dark Chocolate Black Forest Cherries, Chukar Cherries…
Reason: Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Published: December 5, 2018
Distribution: Distributed in AK, AZ, CA, CO, MD, ME, M…

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FDA Recall United States Terminated Historical recordClass I

Chukar Cherry Company

Product: Ultra Dark Chocolate Amaretto Rainier Cherries, Chukar Cherr…
Reason: Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Published: December 5, 2018
Distribution: Distributed in AK, AZ, CA, CO, MD, ME, M…

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FDA Recall United States Terminated Historical recordClass II

ConAgra Foods, INc.

Product: Duncan Hines Signature Confetti Cake cake mix 15.25oz.…
Reason: positive finding of Salmonella in a retail sample
Published: December 5, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

ConAgra Foods, INc.

Product: Duncan Hines Classic Butter Golden cake mix 15.25oz. 12…
Reason: positive finding of Salmonella in a retail sample
Published: December 5, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

ConAgra Foods, INc.

Product: Duncan Hines Classic Classic Yellow cake mix 15.25oz. 1…
Reason: positive finding of Salmonella in a retail sample
Published: December 5, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

ConAgra Foods, INc.

Product: Duncan Hines Classic Classic White cake mix 15.25oz. 12…
Reason: positive finding of Salmonella in a retail sample
Published: December 5, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Red Bull North America Inc.

Product: Red Bull Energy Drink, 8.4 Fl. oz. (250 mL) Ingredient:…
Reason: Investigation of complaints of off taste color and taste found that the product contained 3 times the level of the primary ingredients than is specified in the product formulation.
Published: December 5, 2018
Distribution: DC's in CA, NV, AZ, HI, UT

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FDA Recall Terminated Historical recordClass II

Clopidogrel Tablets, USP, 300 mg, 30 (5 x 6 unit-dose) count blister pack, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Srikakulam - 532 409, India, NDC 55111-671-31

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Dissolution Specification: Out-of-Specification results were observed for dissolution at 18th month stability testing.
Published: November 28, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Medi-Stat Foam, Antimicrobial Hand Soap, Chloroxylenol 0.5%, 1250 mL (42.3 fl oz), OTC, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102, NDC 47593-503-59

by Ecolab Inc

Reason: Labeling: Label mix-up - the label on the product may not match the formula in the bottle.
Published: November 28, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Equi-Soft Foam, Antimicrobial Hand Soap, 0.55% Benzalkonium Chloride, 25 fl oz (750 mL), OTC, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102, NDC 47593-521-41

by Ecolab Inc

Reason: Labeling: Label mix-up - the label on the product may not match the formula in the bottle.
Published: November 28, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals), 100 mg, 100-count Unit Dose Blisters, Rx only, Amerisource Health Services DBA American Health Packaging, 2550-A John Glenn Avenue Columbus, OH 43217, NDC 68084-446-01 (Individual Dose NDC: 68064-446-11)

by American Health Packaging

Reason: Cross contamination with other products: This sub-recall is being initiated in support of the recall by the manufacturer (Sandoz) dated 11/1/18, which included lots that were repackaged by American Health Packaging. Sandoz stated that "These lots are being recalled due to the potential presence of unrelated ingredients (i.e. traces of active ingredients of Benazepril, Haloperidol and Perphenazine), which were identified through a manufacturing investigation."
Published: November 28, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

GSMS Irbesartan Tablets, USP, 300 mg,(a) 30-count bottle (NDC 60429-642-30), (b) 90-count bottle (NDC 60429-642-90), Rx Only, Manufactured by ScieGen Pharmaceuticals, Inc. Hauppauge, NY 11788, Marketed by: GSMS Incorporated Camarillo, CA 93012 USA.

by Sciegen Pharmaceuticals Inc

Reason: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published: November 28, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

GSMS Irbesartan Tablets, USP, 150 mg, (a) 30-count bottle (NDC 60429-641-30), (b) 90-count bottle (NDC 60429-641-90), Rx Only, Manufactured by ScieGen Pharmaceuticals, Inc. Hauppauge, NY 11788, Marketed by: GSMS Incorporated Camarillo, CA 93012 USA.

by Sciegen Pharmaceuticals Inc

Reason: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published: November 28, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

GSMS Irbesartan Tablets, USP, 75 mg, 30-count bottle, Rx Only, Manufactured by ScieGen Pharmaceuticals, Inc. Hauppauge, NY 11788 Marketed by: GSMS Incorporated Camarillo, CA 93012 USA, NDC 60429-640-90.

by Sciegen Pharmaceuticals Inc

Reason: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published: November 28, 2018
Distribution: Nationwide

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Data last updated: September 23, 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.