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Recall totals

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

37,269

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-raw-mild-cheddar-cheese-due-potential-e-coli-o157h7Published October 15, 2026

Most affected stateHawaii 200 recalls mention this state

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

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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

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: August 11, 2025Historical recordClass II

Treehouse Foods

Product: KROGER 12/16.5oz GRDL PNCK ORIG-KROGR UPC 011110811769
Reason: potential to be contaminated with Listeria monocytogenes
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2025Historical recordClass II

Treehouse Foods

Product: H-E-B 12/14.1oz GRDL PNCK MINI HSTYLE ORG-HEBUT UPC 04122098…
Reason: potential to be contaminated with Listeria monocytogenes
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2025Historical recordClass II

Treehouse Foods

Product: KRUSTEAZ 12/15oz GRDL PNCK MINI BTRMLK-KTZCM UPC 68615120016…
Reason: potential to be contaminated with Listeria monocytogenes
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2025Historical recordClass II

Treehouse Foods

Product: SIGNATURE SELECT 12/14.1oz GRDL PNCK MINI-SIGSL UPC 02113009…
Reason: potential to be contaminated with Listeria monocytogenes
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2025Historical recordClass II

Treehouse Foods

Product: SE GROCERS 12/16.5oz GRDL PNCK HSTYLE-SEGGR UPC 038259117194…
Reason: potential to be contaminated with Listeria monocytogenes
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2025Historical recordClass II

Treehouse Foods

Product: GIANT EAGLE 8/33oz GRDL PNCK BTRMLK - GT/EG UPC 030034071332…
Reason: potential to be contaminated with Listeria monocytogenes
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2025Historical recordClass II

Treehouse Foods

Product: BREAKFAST BEST 8/33oz GRDL PNCK BDAY-BKBST UPC 4061459959116
Reason: potential to be contaminated with Listeria monocytogenes
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2025Historical recordClass II

Treehouse Foods

Product: WEGMANS 12/16.5oz GRDL PNCK BB-WEGMN UPC 077890481387 YELLOH…
Reason: potential to be contaminated with Listeria monocytogenes
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2025Historical recordClass II

Treehouse Foods

Product: BREAKFAST BEST 12/12.3oz MXD CS GRDL WFL PMPKN/CINN-BKBST UP…
Reason: potential to be contaminated with Listeria monocytogenes
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2025Historical recordClass II

Treehouse Foods

Product: BREAKFAST BEST 12/13.4oz MXCS GRDL WFL PRTN 6BB 6BM-BKBST
Reason: potential to be contaminated with Listeria monocytogenes
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2025Historical recordClass II

Treehouse Foods

Product: BREAKFAST BEST 12/8 OZ GRDL HSTYLE PLNT BSD WFL-BKBST UPC 40…
Reason: potential to be contaminated with Listeria monocytogenes
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 23, 2026Historical recordClass II

Lisinopril Tablets, USP 10 mg, 90 tablets per bottle, Rx Only, Distributed by: Walmart, Bentonville, AR 72716, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045, NDC# 68645-610-90.

by Evaric Pharmaceuticals Inc.

Reason: Presence of Foreign Object: A pharmacist discovered a metal fragment embedded in a lisinopril 10 mg tablet.
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Docusate Sodium 250 mg, 1 Softgel in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-101-01

by Safecor Health, LLC

Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Calcium Carbonate Chewable 500 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-106-01

by Safecor Health, LLC

Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Aspirin Chewable tablet 81 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-129-01

by Safecor Health, LLC

Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Vitamin B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-108-01

by Safecor Health, LLC

Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-104-01

by Safecor Health, LLC

Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Xelstrym (dextroamphetamine) transdermal system, 13.5 mg dextroamphetamine/9 hours, 30 individually sealed transdermal patches, inside a foil-sealed polypropylene tray, packed in a paper carton/box, MANUFACTURED BY NOVEN PHARMACEUTICALS, INC., Miami, FL 33186 United Sates, NDC 68968-0215-3

by Noven Pharmaceuticals Inc

Reason: Defective Delivery System: The product does not meet predetermined specifications for Coldflow (adhesive).
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 5, 2026Historical recordClass II

Ramipril Capsules USP 10 mg, a) 90 count (NDC 68180-591-09), b) 100 count NDC 68180-591-01), and c) 500 count (NDC 68180-591-02) bottles, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD, Manufactured by Lupin Limited, Goa, India

by Lupin Pharmaceuticals Inc.

Reason: CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 5, 2026Historical recordClass II

Ramipril Capsules USP 5 mg, a) 90 count (NDC 68180-590-09), b) 100 count NDC 68180-590-01), and c) 500 count (NDC 68180-590-02) bottles, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD, Manufactured by Lupin Limited, Goa, India

by Lupin Pharmaceuticals Inc.

Reason: CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
Published: November 27, 2024
Distribution: Nationwide

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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.