Data Explorer

Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,271

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,852

Class I recallsReasonable probability of serious health consequences

24,397

Class II recallsTemporary or medically reversible health consequences

2,897

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 2,085 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 2026

Most affected stateHawaii 200 recalls mention this state

State: MN ×
Clear all

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.

Filters

Timeline Classification Table

Metric

Time range

Group by

View

Recalls announced by month (Year to date)

Download CSV

Source: FDA and USDA public dataLast updated October 17, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

Download CSV

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: February 3, 2026Historical recordClass III

R&M TRADING LLC

Product: Instant Milk Tea Matcha Flavor, R&M Refresher brand, B0D71Y8…
Reason: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published: June 18, 2025
Distribution: Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 3, 2026Historical recordClass III

R&M TRADING LLC

Product: Instant Milk Tea Taro Flavor, R&M Refresher brand, B0D72CMLB…
Reason: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published: June 18, 2025
Distribution: Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 3, 2026Historical recordClass III

R&M TRADING LLC

Product: Instant Milk Tea Honeydew Flavor, R&M Refresher brand, B0D72…
Reason: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published: June 18, 2025
Distribution: Nationwide

View recall →

FDA Recall United States TerminatedTerminated: July 1, 2026Historical recordClass II

NRC Nutrition Pty Ltd

Product: Preconception Multi for Women 60 capsules packaged in bliste…
Reason: inconsistent blending of iodine in the product
Published: June 18, 2025
Distribution: Texas, Minnesota, California, Indiana an…

View recall →

FDA Recall OngoingHistorical recordClass II

Spectrum Advanced Gel Hand Sanitizer, Ethyl alcohol 70%, 8 FL OZ (236 mL) per bottle, Manufactured for Medline Industries, Inc., Three Lakes Drive, Northfield, IL 60693 USA. NDC: 53329-202-08, UPC 8 88277 34945 5

by Consumer Product Partners, LLC

Reason: Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol
Published: June 11, 2025
Distribution: Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Lacosamide Oral Solution, USP, 10 mg/mL, 200 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston FL 33326, NDC 60505-0405-4

by Apotex Corp.

Reason: Defective Container: This recall is being initiated due to a leaking unit stored horizontally.
Published: June 11, 2025
Distribution: Nationwide

View recall →

FDA Recall CompletedHistorical recordClass II

Fluoxetine Tablets, USP, 20 mg, 28-count Carton (4x7 Unit-dose), Manufactured by: TORRENT PHARMACEUTIALS LTD., Indrad-382 721 INDIA; Manufactured for: TORRENT PHARMA INC., Basking Ridge, NJ 07920. NDC: 13668-473-91 (Carton); 13668-473-70 (Blister)

by Torrent Pharma Inc.

Reason: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit.
Published: June 11, 2025
Distribution: Nationwide

View recall →

FDA Recall CompletedHistorical recordClass II

Fluoxetine Tablets, USP, 20 mg, 30-count bottle, Rx only, Manufactured by: TORRENT PHARMACEUTIALS LTD., Indrad-382 721 INDIA; Manufactured for: TORRENT PHARMA INC., Basking Ridge, NJ 07920. NDC: 13668-473-30

by Torrent Pharma Inc.

Reason: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit.
Published: June 11, 2025
Distribution: Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Indomethacin Extended-Release Capsules, USP, 75 mg, 30 capsules (3 x 10 blister cards) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC 68084-411-21 (carton), NDC 68084-411-11 (blister card).

by Amerisource Health Services LLC

Reason: cGMP deviations
Published: June 11, 2025
Distribution: Nationwide

View recall →

FDA Recall United States TerminatedTerminated: December 16, 2025Historical recordClass III

Country Favor Inc.

Product: Best Taste Brand Salted Shrimp Paste Sauce; ING: Shrimp, sug…
Reason: Product contains undeclared FD&C Red #3
Published: June 11, 2025
Distribution: CT, GA, IL, IN KS, KY, LA, MA, MN, MO, M…

View recall →

FDA Recall United States TerminatedTerminated: March 13, 2026Historical recordClass I

South Asian Food Inc.

Product: Bengal King Family Pack Vegetable Singara
Reason: Contains undeclared peanut
Published: June 11, 2025
Distribution: Multiple states

View recall →

FDA Recall United States TerminatedTerminated: June 17, 2025Historical recordClass III

GNC Holdings LLC

Product: GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet…
Reason: Undeclared Fish allergen (parvalbumin).
Published: June 11, 2025
Distribution: The adulterated product was distributed…

View recall →

FDA Recall OngoingHistorical recordClass I

ENDURANCE BOOST WITH HORNY GOAT WEED, 500mg, 20 capsules per carton, VEPEMVA Nutrition Supplement....rgy and Endurance, UPC X004BB9Z8N

by EnShiShiXiangNiShangMaoYouXianGongSi

Reason: Marketed without approved NDA/ANDA: The product has been found to be tainted with Sildenafil and Propoxyphenylsildenafil (a sildenafil analogue).
Published: June 4, 2025
Distribution: Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Theophylline (Anhydrous) Extended-Release Tablets, 600 mg, 100 Tablets per bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited. Colvale-Bardez, Goa - 403513, India. Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC: 68462-356-01

by Glenmark Pharmaceuticals Inc., USA

Reason: OOS results reported for the Dissolution (by UV) test.
Published: June 4, 2025
Distribution: Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Carvedilol Tablets USP 25 mg, 500 -Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC 68462-165-05.

by Glenmark Pharmaceuticals Inc., USA

Reason: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
Published: June 4, 2025
Distribution: Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Carvedilol Tablets USP 12.5 mg, 500-Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC: 68462-164-05

by Glenmark Pharmaceuticals Inc., USA

Reason: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
Published: June 4, 2025
Distribution: Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Carvedilol Tablets USP 6.25 mg, a.)100-count bottle (NDC 68462-163-01), b.) 500-count bottle (NDC 68462-163-05) Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430.

by Glenmark Pharmaceuticals Inc., USA

Reason: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
Published: June 4, 2025
Distribution: Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Carvedilol Tablets USP 3.125mg Tablets a.)100-count bottle (NDC 68462-162-01), b.) 500-count bottle (NDC 68462-162-05), Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430.

by Glenmark Pharmaceuticals Inc., USA

Reason: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
Published: June 4, 2025
Distribution: Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Bromfenac Ophthalmic Solution 0.09%, 1.7 mL bottle, Rx only, Sterile, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, Manufactured by Alembic Pharmaceuticals Limitied, Gujarat, India, Made in India, NDC 62332-508-17

by Alembic Pharmaceuticals Limited

Reason: Failed Impurities/Degradation Specifications
Published: June 4, 2025
Distribution: Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Phentermine Hydrochloride Capsules, USP 30mg, 100-count bottle, Rx Only, Mfd. By: KVK-Tech, Inc., Newtown, PA, 18940, Made in USA, NDC 10702-028-01.

by KVK Tech, Inc.

Reason: cGMP deviations
Published: May 28, 2025
Distribution: Nationwide

View recall →

Data last updated: October 17, 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.