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Recall totals

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

37,118

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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: PR ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 20, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

Westminster Irbesartan Tablets, USP 150 mg Rx Only Manufactured by: ScieGen Pharmaceuticals, Inc. Hauppauge, NY 11788 Manufactured for: Westminster Pharmaceuticals, LLC. Olive Branch, MS 38654 a) 30 count bottle NDC 69367-120-01; b) 90 count bottle NDC 69367-120-03

by Westminster Pharmaceuticals LLC

Reason: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in specific lots of Irbesartan.
Published: December 19, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Westminster Irbesartan Tablets, USP 75 mg Rx Only Manufactured by: ScieGen Pharmaceuticals, Inc. Hauppauge, NY 11788 Manufactured for: Westminster Pharmaceuticals, LLC. Olive Branch, MS 38654 a) 30 count bottle NDC 69367-119-01; b) 90 count bottle NDC 69367-119-03

by Westminster Pharmaceuticals LLC

Reason: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in specific lots of Irbesartan.
Published: December 19, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Thyroid Powder, USP, 25kg/drum, Rx Only, Sichuan Friendly Pharmaceutical Co., LTD. NDC: 070870-1701-1

by LGM Pharma LLC

Reason: CGMP Deviations: Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Published: December 19, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

FastStat Topical Hemostat Introductory Kit, 10% Ferric Sulfate 10%, Rx Only, 3-3cc preloaded syringes. CAO GROUP, INC, 4628 West Skyhawk Drive West Jordan, UT 84084. NDC 1406001003

by CAO Group, Inc.

Reason: cGMP violations noted during the firm's most recent inspection.
Published: December 19, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BeeGentle Honey Flavored Topical Anesthetic, Active ingredient Benzocaine 20%. Packaged in: a) Introductory Kit. Net Qty 3-3cc preloaded syringes. . NDC# 1406000203 UPC 8 72320 00074 5 b) Bulk Kit Net Qty 30mL, NDC# 1406000202, UPC 8 72320 00076 9. Manufactured by CAO (China) Medical Equipment Co. Ltd. for CAO Group, Inc. 4628 West Skyhawk Drive, West Jordan, UT 84084

by CAO Group, Inc.

Reason: cGMP violations noted during the firm's most recent inspection.
Published: December 19, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

SHEER DesenZ Desensitizing Treatment, Rx Only, Potassium Nitrate 12mg per film. CAO GROUP, INC, 4628 West Skyhawk Drive West Jordan, UT 84084. UPC: 8 72320 00072 1 NDC 1406000304

by CAO Group, Inc.

Reason: cGMP violations noted during the firm's most recent inspection.
Published: December 19, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

fas.TRACT Coagulative Hemostatic Gel, 10% Ferric Sulfate Kit, Rx Only, (3) 3cc Preloaded Syringes/ (50) Scrub Tips. Distributed by: Benco Dental, 295 Center Point Blvd., Pittston, PA 18640. NDC: 14060-01105

by CAO Group, Inc.

Reason: cGMP violations noted during the firm's most recent inspection.
Published: December 19, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Feast Mode Blending & Filling

Product: Feast Mode Flavors Garlic Beer Seasoning, Nt. Wt. 5 oz, plas…
Reason: Feast Mode Garlic Beer Seasoning is mislabeled as "Gluten Free"
Published: December 19, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

4Patriots, LLC

Product: 4Patriots Chicken a la King CONTAINS: Wheat, Coconut NET W…
Reason: Milk not declared on product label.
Published: December 19, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Schwan's Global Supply Chain, Inc.

Product: Schwan's Sea Salt Carmel Cashew Ice Cream (#206). Net Wt 56…
Reason: One date of production of Schwan's Sea Salt Caramel Cashew Ice Cream is being due to potential glass contamination.
Published: December 19, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

SODIUM CHLORIDE INJECTION, USP, 0.9%, 20 mL Single Dose Vial, packaged in a 25-unit tray, Rx Only, APP Pharmaceuticals, LLC Schaumburg, IL 60173. NDC 63323-186-20, Product code 918620

by Fresenius Kabi USA, LLC

Reason: Labeling Not Elsewhere Classified: Fresenius Kabi is taking this action due to an incorrect statement on the product insert for product codes 918610 and 918620 indicating that the stoppers do not contain natural rubber latex. The tray label for these two product codes and the vial label for product code 918620 also incorrectly state that the stoppers do not contain latex. The above listed product codes and batches being recalled have stoppers containing natural rubber latex.
Published: December 12, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

SODIUM CHLORIDE INJECTION, USP, 0.9%, 10 mL Single Dose Vial, packaged in a 25-unit tray, Rx Only, APP Pharmaceuticals, LLC Schaumburg, IL 60173. NDC 63323-186-10 Product code 918610

by Fresenius Kabi USA, LLC

Reason: Labeling Not Elsewhere Classified: Fresenius Kabi is taking this action due to an incorrect statement on the product insert for product codes 918610 and 918620 indicating that the stoppers do not contain natural rubber latex. The tray label for these two product codes and the vial label for product code 918620 also incorrectly state that the stoppers do not contain latex. The above listed product codes and batches being recalled have stoppers containing natural rubber latex.
Published: December 12, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/40 mg, Rx only, 30-count bottle, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 0852 Made in India, NDC 65862-855-30

by Aurobindo Pharma USA Inc.

Reason: Discoloration: This product is being recalled due to a confirmed pharmacist report that tablets from this lot were a pink color instead of cream (peach).
Published: December 12, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Agropur MSI Ingredients LLC

Product: Jay Robb Unflavored Egg White Protein, Net Weight 24 oz (1.5…
Reason: JayRobb Unflavored Egg White Protein Product is being recalled due to undeclared milk.
Published: December 12, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Rich Products Corp

Product: VANILLA WHIPPED ICING ARTIFICALLY FLAVORED Product Number: 0…
Reason: Possible contamination with cleaning chemicals.
Published: December 12, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clindamycin Phosphate Topical Solution USP, 1% (10 mg/mL clindamycin), 60 pledget applicators per jar, Rx only. Manufactured by Ei LLC 2865 N. Cannon Blvd. Kannapolis, NC 18083. NDC# 61748-0201-60

by Akorn, Inc.

Reason: Failed Impurities/Degradation Specifications; out of specification results observed for other individual impurities
Published: December 5, 2018
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Sandoz Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 1000-count bottles, Rx Only, Finished Drug Product Manufactured by: Lek Pharmaceuticals d.d. SI-1526 Ljubljana,Sovenia for Sandoz Inc., Princeton, NJ 08540, NDC 0781-5207-10.

by Sandoz, Inc

Reason: CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodiethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of 0.083 parts per million.
Published: December 5, 2018
Distribution: OH and PR

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FDA Recall Terminated Historical recordClass II

Quetiapine Tablets USP 400 mg, 100 tablet bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, India. Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 --- NDC 67877-248-01, UPC code: 3 67877-248-01 1

by Ascend Laboratories LLC

Reason: Presence of Foreign Substance; metal shard found in tablet
Published: December 5, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

ConAgra Foods, INc.

Product: Duncan Hines Signature Confetti Cake cake mix 15.25oz.…
Reason: positive finding of Salmonella in a retail sample
Published: December 5, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

ConAgra Foods, INc.

Product: Duncan Hines Classic Butter Golden cake mix 15.25oz. 12…
Reason: positive finding of Salmonella in a retail sample
Published: December 5, 2018
Distribution: Nationwide

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Data last updated: September 20, 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.