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Recall totals

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

37,118

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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: VT ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 22, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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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FDA Recall Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical recordClass I

Bazzini LLC

Product: BAZZINI S ROASTED & SALTED IN-SHELL PISTACHIOS SUPER COLOSSA…
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 Terminated Historical recordClass I

Euphoric Premium Male Performance Enhancer capsules, packaged in a)1-count blister cards, UPC 6 96859 28646 9, b) 3-count bottle, UPC 6 96859 28647 6 and c) 12-count bottle, UPC 6 96859 28648 3.

by Epic Products, LLC

Reason: Marketed Without An Approved NDA/ANDA: product contains undeclared sildenafil, tadalafil, and oxytetracycline, FDA approved drug products making Euphoric an unapproved drug.
Published: November 21, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Megestrol Acetate Oral Suspension, USP 625 mg/5mL, 150 mL bottle, Rx only, Distributed by: Breckenridge Pharmaceutical, Inc. Boca Raton, FL 33487, Manufactured by: Pharmaceutics International Inc. Hunt Valley, MD 21031

by Breckenridge Pharmaceutical, Inc.

Reason: Failed Stability Specifications: Out-of-Specification results obtained for particle size distribution during stability testing.
Published: November 21, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

children's allergy relief (cetirizine hydrochloride) oral solution, 1 mg/mL, Dye Free, Sugar Free, Alcohol Free, 4 FL OZ (120 mL) bottle, Distributed by Rite-Aid, 30 Hunter Lane, Camp Hill, PA 17011, Made in Israel, UPC 0 11822 57363 4.

by Taro Pharmaceuticals U.S.A., Inc.

Reason: Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
Published: November 21, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

children's allergy (cetirizine hydrochloride) Oral Solution, 1 mg/mL, ANTIHISTAMINE, Dye-Free, Sugar-Free, 4 FL OZ (120 mL) bottle, Distributed by Publix Super Markets, Inc., 3300 Publix Corporate Parkway, Lakeland, FL 33811, NDC 56062-106-08, UPC 0 41415 43573 5.

by Taro Pharmaceuticals U.S.A., Inc.

Reason: Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
Published: November 21, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Children's 24 Hour Allergy (cetirizine hydrochloride) Oral Solution 1 mg/mL, Bubble Gum Flavor, Sugar Free/Dye Free, 4 FL OZ (120 mL) bottle, Dist. by Meijer Distribution, Inc., Grand Rapids, MI 40644, NDC 41250-106-08, UPC 7 13733 88578 2.

by Taro Pharmaceuticals U.S.A., Inc.

Reason: Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
Published: November 21, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals) 100 mg, 100-count bottoles, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141 Manufactured by: Sandoz Inc. Princeton, NJ 08540,NDC 16714-439-01

by Sandoz Inc

Reason: Cross Contamination with Other Products
Published: November 21, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Isosorbide Dinitrate Tablets, USP 20 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-222-00

by Sandoz Inc

Reason: Cross Contamination with Other Products
Published: November 21, 2018
Distribution: Nationwide

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Data last updated: September 22, 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.