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Recall totals

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

37,135

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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 23, 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

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

FDA Recall United States Terminated Historical recordClass II

Ventura Foods, LLC

Product: Smokehouse 220 Sweet & Spicy Barbecue Sauce; Net Wt. 16 OZ.;…
Reason: A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Published: January 24, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods, LLC

Product: Single-serve plastic pack: Newman's Own Lite Sesame Ginger;…
Reason: A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Published: January 24, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods, LLC

Product: Single-serve plastic packet Italian Dressing; Case packing:…
Reason: A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Published: January 24, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods, LLC

Product: plastic cup with foil seal: House Recipe Ranch Dressing & D…
Reason: A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Published: January 24, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods, LLC

Product: plastic cup with foil seal: House Recipe Bleu Cheese Dressi…
Reason: A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Published: January 24, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods, LLC

Product: A&W All American Food Papa Sauce; 8/24 OZ. Pouches; Net Wt 1…
Reason: A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Published: January 24, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods, LLC

Product: Sysco Imperial Tartar Sauce; Net Contents 1 GAL; Distributed…
Reason: A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Published: January 24, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods, LLC

Product: Sysco Imperial Glazed Hot Bacon Dressing; Net Contents 1 GAL…
Reason: A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Published: January 24, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods, LLC

Product: Gordon Choice Honey Mustard Dressing; Net Contents 128 FL OZ…
Reason: A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Published: January 24, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods, LLC

Product: Gordon Choice Thousand Island Dressing; Net Contents 128 FL…
Reason: A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Published: January 24, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods, LLC

Product: Classic Gourmet Dressing; Country French; Net Wt 1.5 OZ.; Ve…
Reason: A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Published: January 24, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Docetaxel Injection USP, 20 mg/mL, One-Vial Formulation, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046 INDIA, NDC 43598-611-11

by Dr. Reddy's Laboratories, Inc.

Reason: Defective Container: Product complaints received of defect in the seal of the Docetaxel injection vials that the aluminum seal and/or stopper is removed when the cap is flipped off.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Gabapentin Oral Solution, 250 mg/5 mL (50 mg/mL) in a 470 mL amber-colored bottle, Rx Only. Manufactured by: Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701. NDC: 50383-311-47

by Akorn Inc

Reason: CGMP Deviations: Inadvertent release of a drug product with unapproved active ingredient manufacturer.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Valsartan Tablets, USP, 160 mg, 90-count bottles, Rx Only, Manufactured by: Zhejiang Huahai Pharmaceutical Co., Ltd, Xunqiao, Linhai, Zhejiang 317024, China; Distributed by: Solco Healthcare US, LLC, Cranbury, NJ 08512, USA; NDC 43547-369-09.

by Prinston Pharmaceutical Inc

Reason: Failed Tablet/Capsule Specifications: confirmed customer complaint of thicker and heavier tablets in bottle.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP, 7.5 mg/12.5 mg, 100-count bottle, Rx only, Distributed By: TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0093-5213-01.

by Teva Pharmaceuticals USA

Reason: Failed Impurities/Degradation Specifications: High out of specification test result for the Moexipril Diketopiperazine impurity was obtained during routine stability testing.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

7-Keto DHEA 25mg Capsule, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.

by KRS Global Biotechnology, Inc

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

7-Ketodehydroepiandrosterone (7-Keto DHEA) 100 mg Capsule, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.

by KRS Global Biotechnology, Inc

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Vitamin 10 B Lyophilized Vial, For IM Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.

by KRS Global Biotechnology, Inc

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Vitamin 9 A/B Lyophilized Vial, For IM Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.

by KRS Global Biotechnology, Inc

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Vitamin 9 Lyophilized Vial, For IM Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.

by KRS Global Biotechnology, Inc

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
Published: January 17, 2018
Distribution: Nationwide

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Data last updated: September 23, 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.