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Recall totals

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

37,059

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/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-healthPublished September 6, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 8, 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

Nivagen, Zinc Oxide Ointment USP, Zinc Oxide 20 %, Net Wt. 1 oz. (28.4g), Nivagen Pharmaceuticals, Inc., Sacramento, CA 95827, USA, Made in India, NDC 75834-170-02.

by Blossom Pharmaceuticals

Reason: cGMP deviations
Published: December 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Nivagen, Zinc Oxide Ointment, Net Wt. 1 oz. (28.4g), Nivagen Pharmaceuticals, Inc., Sacramento, CA 95827, USA Made in India, NDC 75834-170-01.

by Blossom Pharmaceuticals

Reason: cGMP deviations
Published: December 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Dynashield, 4 oz cream (113 g), Manufactured for: Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10852, USA, Made in India, NDC 67777-407-03.

by Blossom Pharmaceuticals

Reason: cGMP deviations
Published: December 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Nivagen Pharmaceuticals, Zinc Oxide Ointment USP, Zinc Oxide 20% Skin Protectant, Net Wt. 15 oz (425g), Made in India, Manufactured for: Nivagen Pharmaceuticals, Inc., Sacramento, CA 95827, USA, NDC 75834-170-15.

by Blossom Pharmaceuticals

Reason: cGMP deviations
Published: December 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

WeCare, Zinc Oxide Ointment, Net Wt. 15 oz/425 g, Manuactured for: Dynarex Corporation, 11 Dynarex Drive, Middletown, NY 10941, Made in India, NDC 67777-223-05.

by Blossom Pharmaceuticals

Reason: cGMP deviations
Published: December 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Dynagel, Moisturizing Wound Hydrogel, Net Wt. 3oz (84.7 g), Manufactured for: Dynarex Corporation, 16 Glenshaw Street, Orangeburg, NY 10962, UPC 61784128016.

by Blossom Pharmaceuticals

Reason: cGMP deviations
Published: December 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Wecare Enema, 4.5 Fl Oz/133mL, Manufactured for: Dynarex Corporation, 11 Dynarex Corporation, MIddletown, NY 10941 USA, Made in India, NDC 67777-402-01.

by Blossom Pharmaceuticals

Reason: cGMP deviations
Published: December 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Dynashield Skin Protectant, Net Wt. 16 oz (453.6 g), Manufactured for: Dyrnarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962, USA, Made in India, NDC 67777-407-04.

by Blossom Pharmaceuticals

Reason: cGMP deviations
Published: December 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Lanashield Skin Barrier, 4 oz. (113 g), Manfuactured for: Dynarex Corporation, 10 Gleshaw Street, Orangeburg, NY 10962 USA, Made in India, UPC 616784126319.

by Blossom Pharmaceuticals

Reason: cGMP deviations
Published: December 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Bisoprolol Fumarate and Hydrochlorothiazide Tablets, USP, 2.5 mg/6.25 mg, packaged as (a) 30-count bottles, NDC-68462-878-30; (b) 100-count bottle, NDC-68462-878-01; (c) 500-count bottles, NDC-68462-878-05; Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, Inda. Manufactured for: Glenmark Pharmaceuticals, Inc., USA, Mahwah, NJ 07430.

by Glenmark Pharmaceuticals Inc., USA

Reason: Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe
Published: December 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Carton label: Testosterone Gel 1%, 2.5 grams per unit dose, CIII, 30 unit-dose packets, Rx only, Manufactured by: Actavis Laboratories, Inc, Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, NDC 0591-3216-30. Packet label: Testosterone Gel 1%, contains 2.5 grams, For topical use only, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054,NDC: 0591-3216-17.

by Teva Pharmaceuticals USA, Inc

Reason: Defective Container - A defect in the side-seal which allows leakage of product.
Published: December 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Phytonadione Injectable Emulsion, USP 10mg/mL, 10x1 mL Single-Dose Vial/carton, Rx Only, Mfd. by: Cipla Ltd. India At M/s Immacule Lifesciences PVT. Ltd. India. Mfd. for: Cipla USA, Inc. Warren, NJ 07059. Vial NDC# 69097-708-31; Carton NDC 69097-708-96

by Cipla Limited

Reason: Failed Stability Specifications: Observed OOS results: eg results for colour index
Published: December 10, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product: Food Club Finely Shredded Pizza Style Four Cheese Blend (con…
Reason: Potential metal fragments from supplier raw material (downstream recall)
Published: December 10, 2025
Distribution: AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass III

Triple B Corporation

Product: COKE FARM Beans, Green 25 lb. Product of USA Coke Farm San J…
Reason: Potential chemical contamination.
Published: December 10, 2025
Distribution: U.S. Distribution: CA, MN, NY, RI

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FDA Recall United States Completed Historical recordClass I

Genepro Protein, Inc.

Product: Genepro Whey 4th Generation Plasma Treated Protein, unflavor…
Reason: Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen
Published: December 10, 2025
Distribution: Multiple states

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FDA Recall United States Ongoing Historical recordClass III

Avion Pharmaceuticals, LLC

Product: Prenate Chewable¿ A chewable Rx prenatal vitamin with a deli…
Reason: Undeclared Soy. The firm received positive test results for soy which is not listed on the label. The firm also noticed that the amount of boron in the product is listed as 250mg per serving instead of 250mcg per serving.
Published: December 10, 2025
Distribution: Product was shipped to the following sta…

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FDA Recall United States Ongoing Historical recordClass II

Laiwu Manhing Vegetables Fruits Co

Product: Onion granules (irradiated) ; 55 lbs carton Item# 5358
Reason: foreign objects (black plastic planting film) in granulated onion powder
Published: December 10, 2025
Distribution: CA

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FDA Recall United States Ongoing Historical recordClass II

Nutrition for Longevity

Product: Loaded Veggie Grain Bowl; NET WT. 10/90 OZ (309g) NO UPC Ide…
Reason: Potential contamination with Listeria monocytogenes.
Published: December 10, 2025
Distribution: Product was shipped directly to consumer…

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FDA Recall United States Terminated Historical recordClass II

Prime Food Processing LLC.

Product: Lava Bun with Salted Egg Yolk orange packaging (Frozen) U…
Reason: Products do not declare milk in the Contains statement or the ingredient statement.
Published: December 10, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Prime Food Processing LLC.

Product: Lava Bun with Green Tea Flavor bright lime green packaging…
Reason: Products do not declare milk in the Contains statement or the ingredient statement.
Published: December 10, 2025
Distribution: Multiple states

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Data last updated: September 8, 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.