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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: WI ×
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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 Ongoing Historical recordClass II

LOSARTAN POTASSIUM TABLETS, USP, 100 mg, a) 90-count (NDC: 13668-115-90), b) 1000-count (NDC: 13668-115-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking Ridge, NJ

by Torrent Pharma Inc.

Reason: CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level.
Published: April 17, 2019
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

LOSARTAN POTASSIUM TABLETS, USP, 50 mg, a) 30-count (NDC: 13668-409-30), b) 90-count (NDC: 13668-409-90), c) 1000-count (NDC: 13668-409-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking Ridge, NJ

by Torrent Pharma Inc.

Reason: CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level.
Published: April 17, 2019
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

LOSARTAN POTASSIUM TABLETS, USP, 25 mg, a) 90-count (NDC: 13668-113-90), b) 1000-count (NDC: 13668-113-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking Ridge, NJ

by Torrent Pharma Inc.

Reason: CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level.
Published: April 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Gavilyte-N, PEG-3350, Sodium chloride, Sodium Bicarbonate and Potassium Chloride for Oral Solution, Rx only, Manufactured by Novel Laboratories, Inc. Somerset, NJ 08873 Manufactured for Lupin Pharmaceuticals, Inc. Baltimore, MD NDC 43386-050-19 UPC 343386050192 a) Lemon Flavor Pack net wt. 2 g UPC 343386200023 b) Orange Flavor Pack net wt. 2 g UPC 343386202027 c) Cherry Flavor Pack net wt. 2 g UPC 3433862034

by LUPIN SOMERSET

Reason: Labeling Not Elsewhere Classified; orange and cherry flavor packets incorrect list "natural lemon flavor" as an ingredient
Published: April 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Life-Line tm Catalytic Activated Energy Water, 1 gallon container, McDaniel Life-Line LLC 1775 US Hwy 385 806-647-1741 Dimmitt, TX 79027

by McDaniel Life-Line LLC

Reason: Unapproved new drug
Published: April 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Indian Herb Paste (a dietary supplement) Ingredients: Galangal, Indian Paint, Yellow Dock & Licorice in an alloy of Life-Line tm and Zinc Chloride in 6 dram vials, McDaniel Life-Line LLC, Dimmitt, TX

by McDaniel Life-Line LLC

Reason: Unapproved new drug
Published: April 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clonidine HCL Injection, 1000 mcg/10mL (100 mcg/mL), 10 ML Single Dose Vial, Rx only, Manufactured for: X-Gen Pharmaceuticals, Big Flats, NY 14814, NDC 39822-2000-1.

by X-Gen Pharmaceuticals Inc.

Reason: Labeling: Label Error on Declared Strength: Side carton panel incorrectly lists the concentration as "500 mcg Clonidine Hydrochloride" rather than the correct concentration of "100 mcg Clonidine Hydrochloride" per mL.
Published: April 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.

by Auro Pharmacies Inc. DBA Central Drugs

Reason: Failed pH Specification: product does not meet pH label claim.
Published: April 17, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Theo Chocolate Inc

Product: Sea Salt 70% Dark Chocolate 3 oz. bars, wrapped in foil and…
Reason: Theo Chocolate Sea Salt 70% Dark Chocolate Bar is recalled due to undeclared milk.
Published: April 17, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

GOOD KARMA FOODS INC

Product: PL Trader Joe Natural Creamer - Vanilla 12/32oz, Plastic bot…
Reason: Product was recalled due to undeclared milk. The Contains statement does not list milk as an ingredient.
Published: April 17, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Merical, LLC

Product: Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsule…
Reason: Incorrect probiotic strain used in formulation which did not match product labeling.
Published: April 17, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Commercial Breader Batter; B95801 BREADER X1; 50 pound b…
Reason: Corn flour which may contain small pieces of plastic.
Published: April 17, 2019
Distribution: Commercial processors in: ALABAMA ARKA…

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Commercial Breader Batter; B95310 BREADER X4; 35 pound b…
Reason: Corn flour which may contain small pieces of plastic.
Published: April 17, 2019
Distribution: Commercial processors in: ALABAMA ARKA…

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Commercial Breader Batter; B94611 BREADER X3; 50 pound b…
Reason: Corn flour which may contain small pieces of plastic.
Published: April 17, 2019
Distribution: Commercial processors in: ALABAMA ARKA…

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Commercial Breader Batter; B93950 BREADER X1; 50 pou…
Reason: Corn flour which may contain small pieces of plastic.
Published: April 17, 2019
Distribution: Commercial processors in: ALABAMA ARKA…

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Commercial Breader Batter; B86044 BATTER MX X1; 50 po…
Reason: Corn flour which may contain small pieces of plastic.
Published: April 17, 2019
Distribution: Commercial processors in: ALABAMA ARKA…

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Commercial Breader Batter; B56666 BREADER X1; 50 po…
Reason: Corn flour which may contain small pieces of plastic.
Published: April 17, 2019
Distribution: Commercial processors in: ALABAMA ARKA…

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Commercial Breader Batter; #52979 BREADER; 50 pound b…
Reason: Corn flour which may contain small pieces of plastic.
Published: April 17, 2019
Distribution: Commercial processors in: ALABAMA ARKA…

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Commercial Breader Batter; B29767 BATTER MX X1; 50 pound b…
Reason: Corn flour which may contain small pieces of plastic.
Published: April 17, 2019
Distribution: Commercial processors in: ALABAMA ARKA…

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Commercial Breader Batter; B28989 BATTER MIX X1; 50 pound…
Reason: Corn flour which may contain small pieces of plastic.
Published: April 17, 2019
Distribution: Commercial processors in: ALABAMA ARKA…

View recall →

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.