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Recall totals

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

37,139

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 25, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass III

Famotidine tablets, 10 mg, packaged in 30-count bottle, OTC, labeled as a) CVS Pharmacy Acid Controller, NDC 55111-118-30, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, Made in India, b) Equate Famotidine, NDC 49035-118-30, Distributed by: Wal-Mart Stores, Inc. Bentonville, AR 72716, Made in India

by Dr. Reddy's Laboratories, Inc.

Reason: Failed impurities/degradation specifications: Famotodine has an out of specification result for an individual related substance observed during routine stability testing of a batch for related substances -impurity 8 at 24 month stability interval.
Published: October 18, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Glutamine, Arginine and Carnitine, 10/100/200mg/mL, 30 mL (Multi Dose Vial), Rx Only, For Injection, United Pharmacy Compounded, 13951 N. Haverhill Rd Ste. 120-121 West Palm Beach, FL 33417

by United Pharmacy

Reason: CGMP Deviations; FDA analysis deterrmined that the product does not contain glutamine and two unknown impurities were observed
Published: October 18, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pinnacle Food Group, Llc

Product: Birds Eye Baby Sweet Peas, Net Wt. 13 oz. (369g ), Keep Froz…
Reason: Product has the potential to be contaminated with Listeria monocytogenes.
Published: October 18, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Silver Spring Foods, Inc.

Product: waterfront Bistro Tatar Sauce, Net Wt 9 oz. (255g), UPC 2113…
Reason: Silver Spring is recalling Waterfront Bistro Tartar Sauce because an incorrect back label does not identify egg.
Published: October 18, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Choice Antibacterial Hand Soap, (ethyl alcohol 61%) 800 ml/ 27 fl oz, Universal Valve, Inopak LTD, Ringwood, NJ

by Inopak Ltd

Reason: GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated diaphragm pump.
Published: October 11, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Mild Healthcare Antibacterial Hand Soap, 6% P.C.M.X., 1000 mL and 2000 mL Disc Pump, 800 mL Universal Valve, and 1 gallon bottles, Inopak. Ltd, Ringwood, NJ 07456

by Inopak Ltd

Reason: GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated diaphragm pump.
Published: October 11, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Option Systems Antibacterial Foaming Hand Wash, 0.3% P.C.M.X., 8 fl oz and 18 fl oz. bottles and 500, mL 800 mL, and 1000 mL pouches, ALSO labeled as STYLE Antibacterial Hand Soap, Inopak Ltd Ringwood, NJ --- NDC 5031-431-02

by Inopak Ltd

Reason: GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated diaphragm pump
Published: October 11, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Deferoxamine Mesylate for injection, USP, Single-use Vial, 500 mg/vial, 10 mL vial. Intravenous, Intramuscular, Subcutaneous Use, Rx Only, Hospira, Inc., Lake Forest IL USA, NDC 0406-2336-10.

by Pfizer Inc.

Reason: CGMP Deviations: Firm failed to control impurity for color change at the API stage.
Published: October 11, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Coborn's, Inc

Product: Coborn's/Cash Wise Caraway Rye Bread - UPC 7-33147-20155-8…
Reason: While reviewing the allergen listings for our products and cross referencing against the updated spec sheet from the manufacturer of the bread base, it was discovered that the allergen statement had been updated from only wheat to wheat, milk, egg and soy.
Published: October 11, 2017
Distribution: Coborn's, Marketplace, and Cashwise stor…

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FDA Recall United States Terminated Historical recordClass II

Coborn's, Inc

Product: Coborn's/Cash Wise American Rye Bread - UPC 7-33147-20150 N…
Reason: Coborn's Inc is recalling packages of its American Rye Bread and Caraway Bread, which contain undeclared allergens (milk, soy, and egg) as a result of an update to the ingredient profile from the manufacturer of the base.
Published: October 11, 2017
Distribution: Coborn's, Marketplace, and Cashwise stor…

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FDA Recall United States Terminated Historical recordClass I

Garden Of Life, LLC

Product: Garden of Life, Baby Organic Liquid probiotic formula, 56 ml…
Reason: The product may pose a choking hazard to newborns due to the thickness of the liquid.
Published: October 11, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pro Bioteks Laboratories

Product: Bio35, Vitamin-Mineral Omega Oils Trace Minerals Dietary Sup…
Reason: Bio-35 has undeclared soy lecithin.
Published: October 11, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

KIND LLC

Product: KIND Dark Chocolate Nuts and Sea Salt Bar-containing 12 /1.…
Reason: Outer box fails to declare the allergen walnuts, the individual bar is properly labeled
Published: October 11, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Ampicillin for Injection, USP, 500 mg per vial, single vial (NDC 0781-3407-78) packaged in 10-count shrink wrap packs (NDC 0781-3407-95), Rx only, Manufactured in Austria by Sandoz GmbH or Sandoz Inc., Princeton, NJ 08540.

by Sandoz Inc

Reason: Labeling: Missing Label: customer complaint that some vials of ampicillin within the shrink wrap pack are missing labels.
Published: October 4, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Acarbose Tablets, 25 mg, 100-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; NDC 16252-523-01.

by Teva Pharmaceuticals USA

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: An incorrect expiration date of July 2018 is printed on the product labeling rather than the correct expiration date of July 2017.
Published: October 4, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc., South San Francisco, CA 94080-4990. NDC 50242-901-24

by Pfizer Inc.

Reason: Non-Sterility: cracked or chipped glass at the neck of Sterile Water for Injection vials.
Published: October 4, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

House Of Thaller Inc

Product: Marketside CLASSIC HUMMUS WITH PINE NUTS NET WT. 10 oz (283g…
Reason: The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

House Of Thaller Inc

Product: LANTANA White Bean HUMMUS NET WT. 10 oz (283g)
Reason: The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

House Of Thaller Inc

Product: FRESH FOODS MARKET Artisan Humus Pine Nuts NET WT 10 oz (283…
Reason: The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Product was shipped to the following sta…

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FDA Recall Terminated Historical recordClass I

Activase (alteplase), 100 mg (58 million IU), Lyophilized vial, packaged with 1 single-dose 100ml vial of sterile water for Injection USP and one transfer device. Manufactured by: Genentech, Inc. 1 DNA Way, South San Francisco, CA 84080-4990. NDC: 50242-0085-27

by Genentech, Inc.

Reason: Non-Sterility:presence of cracked or chipped glass at the neck of Sterile Water for Injection vials.
Published: September 27, 2017
Distribution: Nationwide

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Data last updated: September 25, 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.