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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

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 8, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall OngoingHistorical recordClass II

Amlodipine and Valsartan Tablets, USP, 10 mg/160mg, 30 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-206-30

by Torrent Pharma Inc.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Amlodipine and Valsartan Tablets, USP, 5 mg/320 mg, 30 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-205-30

by Torrent Pharma Inc.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Amlodipine and Valsartan Tablets, USP, 10 mg/320 mg, 30 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-204-30

by Torrent Pharma Inc.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Valsartan Tablets USP, 320mg, 90 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-070-90

by Torrent Pharma Inc.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Valsartan Tablets USP, 160mg, 90 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-069-90

by Torrent Pharma Inc.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Valsartan Tablets USP, 80mg, 90 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-068-90

by Torrent Pharma Inc.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II

Valsartan Tablets, USP 320 mg Rx Only 30 Tablets (6x5) Unit Dose NDC 50268-786-13 Manufactured for: AvKARE, Inc. Pulaski, TN 38478

by AVKARE Inc.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II

Valsartan Tablets, USP 160 mg Rx Only 50 Tablets (5x10) Unit Dose NDC 50268-785-15 Manufactured for: AvKARE, Inc. Pulaski, TN 38478

by AVKARE Inc.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II

Valsartan Tablets, USP 80 mg Rx Only 50 Tablets (5x10) Unit Dose NDC 50268-784-15 Manufactured for: AvKARE, Inc. Pulaski, TN 38478

by AVKARE Inc.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II

Valsartan Tablets, USP 40 mg Rx Only NDC 50268-783-15 50 Tablets (5x10) Unit Dose Manufactured for: AvKARE, Inc. Pulaski, TN 38478

by AVKARE Inc.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 19, 2020Historical recordClass III

Oxycodone and Acetaminophen Tablets, USP, 5 mg*/325 mg, 100-count bottle, Rx Only, Manufactured by: Mayne Pharma, Greenville, NC 27834, NDC 68308-841-01.

by Mayne Pharma Inc

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: Lot FG10517 is mislabeled on the primary container with Lot FG01517, shipper labels and invoices contain the correct lot number of FG10517.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II

Doxycycline Hyclate USP Tablets, 100 mg packaged in a) 2-count bottles, NDC 55289-866-02; b) 6-count bottles, NDC 55289-866-06; c) 7-count bottles, NDC 55289-866-07; d) 10-count bottles, NDC 55289-866-10; e) 14-count bottles, NDC 55289-866-14; f) 20-count bottles, NDC 55289-866-20; g) 28-count bottles, NDC 55289-866-28; h) 30-count bottles, NDC 55289-866-30; i) 120-count bottles, NDC 55289-866-98; j) 300-count bottles, NDC 55289-866-87; k) 400-count bottles, NDC 55289-866-74; Rx only, Packaged By PD-Rx Pharmaceuticals, Oklahoma City, OK 73127.

by PD-Rx Pharmaceuticals, Inc.

Reason: Failed Dissolution Specifications: manufacturer West-Ward Pharm Corp. recalled these repackaged lots due to failed dissolution results.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 21, 2018Historical recordClass II

Lipari Foods Operating Company, LLC dba JLM Manufacturing

Product: Premo Brand Turkey & Cheese Wedge sandwiches 5 OZ retail…
Reason: Potential contamination of Listeria monocytogenes
Published: September 5, 2018
Distribution: Distributed to food service and retail s…

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FDA Recall United States TerminatedTerminated: March 8, 2019Historical recordClass III

MORTON SALT INC

Product: MORTON NATURAL SEA SALT ALL PURPOSE***NET WET 26 OZ (1 LB 10…
Reason: Iodized sea salt was packaged in Morton Natural Sea Salt packages.
Published: September 5, 2018
Distribution: Products were distributed in the followi…

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FDA Recall United States TerminatedTerminated: December 18, 2018Historical recordClass II

Hostess Brands, LLC

Product: Hostess Brownies Cookies 'n Cr¿me packaged in the following…
Reason: The product ingredients statement declares egg ingredients, but the "Contains" statement fails to declare egg.
Published: September 5, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 3, 2020Historical recordClass I

Levothyroxine and Liothyronine (Thyroid Tablets, USP), 2 grain (120 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-158-04.

by Westminster Pharmaceuticals LLC

Reason: Failed Content Uniformity Specifications: Product was manufactured using an adulterated active pharmaceutical ingredient; additionally, lack of process controls and good manufacturing practices resulted in finished product failing content uniformity specifications which can result in a product having a strength that is more or less than is labeled.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 3, 2020Historical recordClass I

Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1/4 grain (15 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-159-04.

by Westminster Pharmaceuticals LLC

Reason: Failed Content Uniformity Specifications: Product was manufactured using an adulterated active pharmaceutical ingredient; additionally, lack of process controls and good manufacturing practices resulted in finished product failing content uniformity specifications which can result in a product having a strength that is more or less than is labeled.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 3, 2020Historical recordClass I

Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1/2 grain (30 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-155-04.

by Westminster Pharmaceuticals LLC

Reason: Failed Content Uniformity Specifications: Product was manufactured using an adulterated active pharmaceutical ingredient; additionally, lack of process controls and good manufacturing practices resulted in finished product failing content uniformity specifications which can result in a product having a strength that is more or less than is labeled.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 3, 2020Historical recordClass I

Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1 & 1/2 grain (90 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-157-04.

by Westminster Pharmaceuticals LLC

Reason: Failed Content Uniformity Specifications: Product was manufactured using an adulterated active pharmaceutical ingredient; additionally, lack of process controls and good manufacturing practices resulted in finished product failing content uniformity specifications which can result in a product having a strength that is more or less than is labeled.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 3, 2020Historical recordClass I

Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1 grain (60 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-156-04.

by Westminster Pharmaceuticals LLC

Reason: Failed Content Uniformity Specifications: Product was manufactured using an adulterated active pharmaceutical ingredient; additionally, lack of process controls and good manufacturing practices resulted in finished product failing content uniformity specifications which can result in a product having a strength that is more or less than is labeled.
Published: August 29, 2018
Distribution: Nationwide

View recall →

Data last updated: November 8, 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.