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Recall totals

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

37,449
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Most affected stateHawaii 200 recalls mention this state

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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)

  • 1,956 recalls have been announced year to date.
  • Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
  • Nov 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 II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 11,881–11,900 of 21,307 recalls

FDA Recall United States TerminatedTerminated: October 22, 2020Historical 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 TerminatedTerminated: October 22, 2020Historical 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 TerminatedTerminated: October 22, 2020Historical 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 TerminatedTerminated: October 22, 2020Historical 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 TerminatedTerminated: March 28, 2019Historical recordClass II

Chicago Importing Co

Product
Finax Muesli with 45% Fruit; 22.9-oz.; Heat sealed plastic…
Reason
The product's ingredients statement does not indicate presence of coconut
Published
December 5, 2018
Distribution
AZ CA FL IL MA MD MI MN NJ NY…

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FDA Recall TerminatedTerminated: May 19, 2020Historical 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 TerminatedTerminated: November 6, 2020Historical 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 TerminatedTerminated: November 6, 2020Historical 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 TerminatedTerminated: September 30, 2020Historical 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 TerminatedTerminated: September 25, 2023Historical 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 TerminatedTerminated: September 25, 2023Historical 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 TerminatedTerminated: September 25, 2023Historical 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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FDA Recall TerminatedTerminated: September 25, 2023Historical recordClass II

Westminister Irbesartan Tablets, USP, 300mg, Rx Only,(a) 30-count bottle (NDC 69367-121-01, (b) 90-count bottle (NDC 69367-121-03), Manufactured by ScieGen Pharmaceuticals Inc. Hauppauge, NY 11755. Manufactured for Westminster Pharmaceuticals LLC Olive Branch, MS 20854 Made in the 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 TerminatedTerminated: September 25, 2023Historical recordClass II

Westminister Irbesartan Tablets, USP, 150 mg, (a) 30-count bottle (NDC 69367-120-01), (b) 90-count bottle (NDC 69367-120-03), Rx Only, Manufactured by ScieGen Pharmaceuticals Inc. Hauppauge, NY 11755, Manufactured for Westminster Pharmaceuticals LLC Olive Branch, MS 20854, Made in the 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 TerminatedTerminated: September 25, 2023Historical recordClass II

Westminister Irbesartan Tablets, USP, 75 mg (a) 30-count bottle (NDC 69367-119-01), (b) 90-count bottle (NDC 69367-119-03), Rx Only, Manufactured by ScieGen Pharmaceuticals Inc Hauppauge, NY 11755 Manufactured for Westminister Pharmaceuticals LLC Olive Branch, MS 20854 Made in the 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 TerminatedTerminated: September 28, 2020Historical recordClass II

Antacid Tablets, Calcium Carbonate chewable tablets, 750mg, 60-count bottle, OTC, [Healthy Accents brand NDC: 55316-014-72, Distributed by DZA Brands, LLC, Salisbury, NC 28147, Scarborough, ME 04074], [HealthMart Pharmacy brand NDC: 62011-0295-1, Distributed by McKessen, One Post Street, San Francisco, CA 94104], [DG health brand NDC: 55910-717-72, Distributed By Dolgencorp, LLC, 100 Mission Ridge, Goodlettsville, TN 37072]

by L. Perrigo Company

Reason
Presence of foreign substance: Product found to contain metal particles.
Published
November 28, 2018
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 15, 2022Historical recordClass I

Bazzini LLC

Product
BAZZINI S ROASTED & SALTED IN-SHELL PISTACHIOS COLOSSAL NATU…
Reason
The product tested positive for Salmonella.
Published
November 28, 2018
Distribution
Product has been shipped to the followin…

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FDA Recall United States TerminatedTerminated: March 15, 2022Historical recordClass I

Bazzini LLC

Product
BAZZINIS ROASTED & SALTED IN-SHELL PISTACHIOS RAMS HEAD NATU…
Reason
The product tested positive for Salmonella.
Published
November 28, 2018
Distribution
Product has been shipped to the followin…

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FDA Recall United States TerminatedTerminated: March 15, 2022Historical recordClass I

Bazzini LLC

Product
BAZZINI S ROASTED & SALTED IN-SHELL SUPER COLOSSAL PISTACHIO…
Reason
The product tested positive for Salmonella.
Published
November 28, 2018
Distribution
Product has been shipped to the followin…

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FDA Recall United States TerminatedTerminated: March 15, 2022Historical recordClass I

Bazzini LLC

Product
BAZZINI S ROASTED & SALTED IN-SHELL PISTACHIOS COLOSSAL NATU…
Reason
The product tested positive for Salmonella.
Published
November 28, 2018
Distribution
Product has been shipped to the followin…

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.

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