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Recall totals

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

37,063

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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 2,072 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 11, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Ongoing Historical 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 Terminated Historical recordClass II

HydrALAZINE Hydrochloride Tablets, USP 10mg, packaged in 100-count (10x10 blister cards), Lot T04680, Rx only, Manufactured for Heritage Pharmaceuticals, Inc. Eatontown, NJ, Distributed by Major Pharmaceuticals Livonia MI. NDC 0904-6440-61

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

Reason: an out of specification result obtained during routine stability testing for Impurities. There is a remote possibility that use of this product could cause a medically reversible or transient adverse health consequences.
Published: February 21, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Nortrel 7/7/7 (norethindrone and ethinyl estradiol tablets USP- triphasic regimen), packaged in cartons, each carton contains 6 blister cards, each card contains 28 tablets, Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0555-9012-58

by Teva Pharmaceuticals USA, Inc

Reason: Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
Published: February 21, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35, packaged in cartons, each carton contains 3 blister cards, each card contains 28 tablets, Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0555-9008-67

by Teva Pharmaceuticals USA, Inc

Reason: Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
Published: February 21, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

UNFI General Corporate

Product: Woodstock 5 Grain Cereal. Oats, Rye, Triticale, Barley, Gol…
Reason: The ingredient Triticale is not identified as wheat.
Published: February 21, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

U.S. Tov, Inc.

Product: Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557…
Reason: Potential choking hazard; product contains konjac.
Published: February 21, 2024
Distribution: U.S. distribution to the following: AK,…

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FDA Recall Ongoing Historical recordClass III

HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100-count (10 x 10) per unit dose carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 68084-447-01; NDC Unit Dose: 68084-447-11

by Amerisource Health Services LLC

Reason: Failed Impurities/Degradation Specifications: Out of Specification (OOS) result in the repackaged product for Related Compounds (Impurities) at the 6-month time point.
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Phenoxybenzamine Hydrochloride Capsules, USP 10mg, 100-count bottle, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd, Oral Solid Dosage Unit, Ahmedabad 382213, India, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 60219-1502-01

by Amneal Pharmaceuticals of New York, LLC

Reason: Failed Impurities/Degradation Specifications: Out of specification for unknown impurity.
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lansoprazole Delayed-Release Capsules USP, 15 mg, 14-count bottle, Manufactured by: Natco Pharma Limited Kothur- 509 228, India, Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ. 08816. NDC 16571-742-41

by NATCO Pharma Limited

Reason: CGMP Deviations: Inadequate induction sealing on bottles, capsules were observed with bubbles on band seal, capsules with holes and spheres sticking to capsules. Also coding details were missing on one bottle.
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Medline Remedy Clinical TREAT Antifungal Cream, 2% Miconazole Nitrate, Paraben Free, 4 FL OZ (118 mL) tube, Manufactured for Medline Industries, LP Three Lakes Drive, Northfield, IL 60093. NDC: 53329-147-44

by MEDLINE INDUSTRIES, LP - Northfield

Reason: Labeling: Not Elsewhere Classified; Product labeling contains the claim of 'Paraben Free' while the product does in fact contain parabens as part of the formulation/ ingredient list.
Published: February 14, 2024
Distribution: Nationwide

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Data last updated: September 11, 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.