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Recall totals

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

37,142

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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 27, 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 Terminated Historical recordClass II

Losartan Potassium, 50 mg tablets, 90 count bottle, NDC 60429-317-90

by Golden State Medical Supply Inc.

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium, 50 mg tablets, 30 count bottle, NDC 60429-317-30

by Golden State Medical Supply Inc.

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium andHydrochlorothiazide Tablets 100 mg/25 mg 90 tablets, USP Rx Only, Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-052-10

by Macleods Pharma Usa Inc

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/12.5 mg 90 Tablets, USP Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-051-10

by Macleods Pharma Usa Inc

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium and Hydrochlorothiazide Tablets, USP 50 mg/12.5 mg 90 Tablets, USP Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-050-10

by Macleods Pharma Usa Inc

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets 50 mg 1000 Tablets, USP Rx Only Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-045-44

by Macleods Pharma Usa Inc

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets, USP 50 mg 90 tablets Rx Only Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-045-10

by Macleods Pharma Usa Inc

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

LOSARTAN POTASSIUM 100 mg TABLET BULK 90 count bottles, NDC 00591-3747-00

by Teva Pharmaceuticals USA

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

LOSARTAN POTASSIUM 50 mg TABLET BULK 90 count bottles and 1000 count bottles, NDC 00591-3746-00

by Teva Pharmaceuticals USA

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ziba Nut Incorporated

Product: OU Kosher Salted and Roasted Edamame Green Beans (Regular Sa…
Reason: Product does not declare soy. Allergen statement not printed on label of roasted and salted Edamame.
Published: July 17, 2019
Distribution: Multiple states

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FDA Recall United States Ongoing Historical recordClass II

Riverside Foods Llc

Product: Tipton Grove Frozen Mixed Berries NET WT 12 OZ (340g) bags D…
Reason: The firm was informed by their customer that a random sample tested by the FDA test positive for norovirus.
Published: July 17, 2019
Distribution: Distribution went to Wal-Mart and Save-A…

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FDA Recall United States Ongoing Historical recordClass II

Riverside Foods Llc

Product: Great Value Blackberries NET WT 16 OZ (1 LB) 454g bags DISTR…
Reason: The firm was informed by their customer that a random sample tested by the FDA test positive for norovirus.
Published: July 17, 2019
Distribution: Distribution went to Wal-Mart and Save-A…

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FDA Recall United States Terminated Historical recordClass I

Baumer Foods Inc

Product: Soy Sauce, 10 FL OZ
Reason: Undeclared allergen. Worcestershire sauce mislabeled as soy sauce.
Published: July 17, 2019
Distribution: Distributed to The Golub Corp. Sold in…

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FDA Recall United States Terminated Historical recordClass II

Stagno's Bakery, Inc.

Product: Stagno's Bakery, Inc., P005, Grain Bagel , Contains Wheat, S…
Reason: Stagno's Bakery, Inc. initiated a recall on 05/24/2019 of wholesale frozen bagel dough / bulk to one direct account because the product is potentially contaminated with E. Coli .
Published: July 17, 2019
Distribution: The product was shipped to Schenectady,…

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FDA Recall United States Terminated Historical recordClass II

Stagno's Bakery, Inc.

Product: Stagno's Bakery, Inc., P016, Spinach Garlic Bagel , Contains…
Reason: Stagno's Bakery, Inc. initiated a recall on 05/24/2019 of wholesale frozen bagel dough / bulk to one direct account because the product is potentially contaminated with E. Coli .
Published: July 17, 2019
Distribution: The product was shipped to Schenectady,…

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FDA Recall United States Terminated Historical recordClass II

Stagno's Bakery, Inc.

Product: Stagno's Bakery, Inc., P015, Pumpernickel Bagel , Contains W…
Reason: Stagno's Bakery, Inc. initiated a recall on 05/24/2019 of wholesale frozen bagel dough / bulk to one direct account because the product is potentially contaminated with E. Coli .
Published: July 17, 2019
Distribution: The product was shipped to Schenectady,…

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FDA Recall United States Terminated Historical recordClass II

Stagno's Bakery, Inc.

Product: Stagno's Bakery, Inc., P001, Plain Bagel , Contains Wheat, S…
Reason: Stagno's Bakery, Inc. initiated a recall on 05/24/2019 of wholesale frozen bagel dough / bulk to one direct account because the product is potentially contaminated with E. Coli .
Published: July 17, 2019
Distribution: The product was shipped to Schenectady,…

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FDA Recall United States Terminated Historical recordClass II

Stagno's Bakery, Inc.

Product: Stagno's Bakery, Inc., P018, Jalapeno Bagel , Contains Wheat…
Reason: Stagno's Bakery, Inc. initiated a recall on 05/24/2019 of wholesale frozen bagel dough / bulk to one direct account because the product is potentially contaminated with E. Coli .
Published: July 17, 2019
Distribution: The product was shipped to Schenectady,…

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FDA Recall United States Terminated Historical recordClass II

Stagno's Bakery, Inc.

Product: Stagno's Bakery, Inc., P014, Honey Wheat Bagel , Contains Wh…
Reason: Stagno's Bakery, Inc. initiated a recall on 05/24/2019 of wholesale frozen bagel dough / bulk to one direct account because the product is potentially contaminated with E. Coli .
Published: July 17, 2019
Distribution: The product was shipped to Schenectady,…

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FDA Recall United States Terminated Historical recordClass II

Stagno's Bakery, Inc.

Product: Stagno's Bakery, Inc., P011, Egg Bagel , Contains Wheat, Soy…
Reason: Stagno's Bakery, Inc. initiated a recall on 05/24/2019 of wholesale frozen bagel dough / bulk to one direct account because the product is potentially contaminated with E. Coli .
Published: July 17, 2019
Distribution: The product was shipped to Schenectady,…

View recall →

Data last updated: September 27, 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.