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Recall totals

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

37,343

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/vitality-works-inc-recalls-365-whole-foods-market-ashwagandha-capsules-sold-nationwide-due-potentialPublished October 30, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 30, 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 CompletedHistorical recordClass II

Adrenalin (epinephrine) Injection 1mg/mL, 1mL single dose vial, Rx only, Packaged By: Henry Schein, Inc., 80 Summit View Lane, Bastian, VA 24314, Original NDC 42023-159-25 Repack NDC 0404-9810-01

by Henry Schein Inc. and Glove Club HSI Gloves Inc.

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is incorrect.
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Terlivaz (terlipressin for injection), 0.85mg/vial, Single-Dose Vial, Rx only, Distributed by: Mallinckrodt Hospital Products Inc., Bridgewater, NJ 08807, USA, NDC 43825-200-01

by Mallinckrodt Hospital Products Inc.

Reason: cGMP deviations: Temperature excursion due to shipping delay from manufacturer to distributor. Affected distributor has been notified.
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Acthar Gel (repository corticotropin injection) 400 USP units/5mL (80 USP units/mL), 5mL multiple-dose vial, Rx only, Mfd. for: Mallinckrodt ARD LLC, Bridgewater, NJ 08807, NDC 63004-8710-1

by Mallinckrodt Hospital Products Inc.

Reason: cGMP deviations: Temperature excursion due to shipping delay from manufacturer to distributor. Affected distributor has been notified.
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Fosfomycin Tromethamine Granules for Oral Solution, (equivalent to 3 grams of fosfomycin), single-dose sachet, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA. Distributed by: Ascend Laboratories, LLC. Parsippany, NJ 07054. NDC 67877-749-57

by Ascend Laboratories, LLC

Reason: Failed Impurities/Degradation Specification: Out of specification for organic impurities
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Norepinephrine Bitartrate in 5% Dextrose Injection, 8 mg/ 250 mL (32 mcg/mL), For Intravenous Infusion Only, 250 mL vial, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015. Made in Ireland. NDC: 0338-0108-20

by Baxter Healthcare Corporation

Reason: Incorrect product concentration on the overwrap label: The overwrap label incorrectly identified the product strength as 4 mg / 250 mL; however, the primary bag label correctly identified the product strength as 8 mg / 250 mL.
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Neptune's Fix, Tianeptine Tablets Extended Relief, Twenty Tablets per Box, Wide Awake, 3000 mg (150 mg Per Tablet), Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.

by Neptune Resources, LLC

Reason: Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Neptune's Fix, Tianeptine Extra Strength Elixir, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.

by Neptune Resources, LLC

Reason: Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.

by Neptune Resources, LLC

Reason: Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 9, 2026Historical recordClass II

Equate Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, a) 30 drops per bag, item number 20000462, b) 160 drops per bag, item number 20000463, Bestco, 288 Mazeppa Road, Mooresville, NC 28115

by Bestco LLC

Reason: CGMP Deviations: Potential Glass and Silicone particulates in product
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 9, 2026Historical recordClass II

Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic, 80 drops per bag, item number 20001187, Bestco, 288 Mazeppa Road, Mooresville, NC 28115

by Bestco LLC

Reason: CGMP Deviations: Potential Glass and Silicone particulates in product
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 9, 2026Historical recordClass II

Kroger Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per bag, item number 20000064, Bestco, 288 Mazeppa Road, Mooresville, NC 28115

by Bestco LLC

Reason: CGMP Deviations: Potential Glass and Silicone particulates in product
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 9, 2026Historical recordClass II

Meijer Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per bag, item number 20000345, Bestco, 288 Mazeppa Road, Mooresville, NC 28115

by Bestco LLC

Reason: CGMP Deviations: Potential Glass and Silicone particulates in product
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 9, 2026Historical recordClass II

CVS Health Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 160 drops per bag, item number 20001089, Bestco, 288 Mazeppa Road, Mooresville, NC 28115

by Bestco LLC

Reason: CGMP Deviations: Potential Glass and Silicone particulates in product
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 14, 2025Historical recordClass II

Oseltamivir Phosphate for Oral Suspension 6mg/ml, 60 mL (reconstituted) bottle, RX only, Distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807. NDC# 69238-1273-6

by Amneal Pharmaceuticals of New York, LLC

Reason: Failed Impurities/Degradation Specifications: Out-of-specification test results.
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Fluticasone Propionate Nasal Spray USP 50mcg, 120 Metered Sprays - 16 g net fill, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9, Manufactured for: Apotex Corp Weston, FL 33326. NDC 60505-0829-1

by Apotex Corp.

Reason: CGMP Deviations: potential presence of Burkholderia cepacia complex
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: November 21, 2025Historical recordClass II

The Procter & Gamble Company

Product: Meta Psyllium Fiber Capsules packaged as 100 count or 160 co…
Reason: Illegible Label
Published: February 28, 2024
Distribution: Alabama, Arizona, Arkansas, California,…

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FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II

Mennel Milling Company

Product: PIZZA 50/50 UNMALTED 904181 delivered as bulk product in app…
Reason: Potential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
Published: February 28, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II

Mennel Milling Company

Product: PB AP delivered as bulk product in approximately 50,000 lbs…
Reason: Potential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
Published: February 28, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II

Mennel Milling Company

Product: NON-HUMAN CONSUMPTION delivered as bulk product in approxima…
Reason: Potential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
Published: February 28, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 21, 2024Historical recordClass II

Mennel Milling Company

Product: I-52 PATENT FLOUR delivered as bulk product in approximately…
Reason: Potential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
Published: February 28, 2024
Distribution: Multiple states

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Data last updated: October 30, 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.