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Recall totals

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

37,341

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,860

Class I recallsReasonable probability of serious health consequences

24,450

Class II recallsTemporary or medically reversible health consequences

2,901

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 2,095 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/haifa-smoked-fish-recalls-cold-smoked-sprats-due-potential-health-riskPublished October 27, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 28, 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	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

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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FDA Recall TerminatedTerminated: January 5, 2026Historical recordClass II

Ramipril Capsules USP 2.5 mg, a) 90 count (NDC 68180-589-09), b) 100 count NDC 68180-589-01), and c) 500 count (NDC 68180-589-02) 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: March 28, 2025Historical recordClass II

BEVACIZUMAB (AVASTIN)1.25mg/0.05mL, Sterile Injection, 0.5 mL Single-Dose Syringe, Rx Only, Repackaged by: Medivant Healthcare: 24416 N 19th Ave, Phoenix, AZ, NDC 81483-0041-1

by Tailstorm Health INC

Reason: Lack of Sterility Assurance
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 5, 2026Historical recordClass II

Guaifenesin Dextromethorphan Syrup, 100 mg/10mg per 5 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7134-70

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason: Failed Impurity/Degradation Specifications
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 5, 2026Historical recordClass II

Guaifenesin Dextromethorphan Syrup, 200 mg/20mg per 10 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7135-72

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason: Failed Impurity/Degradation Specifications
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 29, 2025Historical recordClass III

Triamcinolone Acetonide Cream USP, 0.025%, 1 LB (454 g) per jar, Rx Only, Manufactured By Padagis, Minneapolis, MN 55427. NDC: 45802-0063-05

by Padagis US LLC

Reason: Subpotent and Superpotent Drug. Out of specification assay results recorded as part of Uniformity of Container test during long-term stability testing.
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass III

IBU (ibuprofen) 600 mg tablets, 500-count bottle, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-683-05

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Tablet/Capsule Specifications
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 17, 2026Historical recordClass I

Grand Central Bakery FRE Co Inc

Product: U-BAKE Chicken Pot Pie, frozen product and packaged in heat-…
Reason: Undeclared egg
Published: November 27, 2024
Distribution: Distributed in OR and WA.

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FDA Recall United States TerminatedTerminated: March 17, 2026Historical recordClass I

Grand Central Bakery FRE Co Inc

Product: U-BAKE Marionberry Pie, frozen product and packaged in LDPE…
Reason: Undeclared egg
Published: November 27, 2024
Distribution: Distributed in OR and WA.

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FDA Recall United States TerminatedTerminated: March 17, 2026Historical recordClass I

Grand Central Bakery FRE Co Inc

Product: U-BAKE Pie Crust (Pastry Round), frozen product and packaged…
Reason: Undeclared egg
Published: November 27, 2024
Distribution: Distributed in OR and WA.

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FDA Recall United States TerminatedTerminated: March 17, 2026Historical recordClass I

Grand Central Bakery FRE Co Inc

Product: U-BAKE Apple Pie, frozen product and packaged in LDPE bag, n…
Reason: Undeclared egg
Published: November 27, 2024
Distribution: Distributed in OR and WA.

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FDA Recall United States TerminatedTerminated: February 6, 2025Historical recordClass II

SAVENCIA CHEESE USA

Product: Glenview Farms Spreadable Brie 2, 3lb tubs per case
Reason: potential to be contaminated with Listeria monocytogenes
Published: November 27, 2024
Distribution: CA CO CT IA IL IN MA MO NJ OR TX WA

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FDA Recall United States TerminatedTerminated: February 6, 2025Historical recordClass II

SAVENCIA CHEESE USA

Product: La Bonne Vie Camembert 8oz UPC 820581678616; 6 retail units…
Reason: potential to be contaminated with Listeria monocytogenes
Published: November 27, 2024
Distribution: CA CO CT IA IL IN MA MO NJ OR TX WA

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FDA Recall United States TerminatedTerminated: February 6, 2025Historical recordClass II

SAVENCIA CHEESE USA

Product: Aldi Emporium Selection Brie 8oz UPC 4099100084016; 12 retai…
Reason: potential to be contaminated with Listeria monocytogenes
Published: November 27, 2024
Distribution: CA CO CT IA IL IN MA MO NJ OR TX WA

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FDA Recall United States TerminatedTerminated: February 4, 2025Historical recordClass I

Joseph Seviroli, LLC

Product: Chicken Alfredo Kit
Reason: Contains chicken contaiminated with Listeria monocytogenes
Published: November 27, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 13, 2025Historical recordClass II

The JM Smucker Company LLC

Product: Great Value Cinnamon Rolls 16.5oz UPC 078742201160, 12 retai…
Reason: Pieces of plastic in product
Published: November 27, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 13, 2025Historical recordClass II

The JM Smucker Company LLC

Product: Great Value Cheese Danish 16.5 oz UPC 078742201177, 12 retai…
Reason: Pieces of plastic in product
Published: November 27, 2024
Distribution: Nationwide

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Data last updated: October 28, 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.