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Recall totals

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

37,115

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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 16, 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 III

Allergy & Congestion Relief Allergy Relief D, Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Tablets, 20 extended-release tablets, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, Made in India, NDC 69842-249-20

by Dr. Reddy's Laboratories, Inc.

Reason: Failed dissolution specifications
Published: December 15, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Allergy & Congestion Fexofenadine HCl 60 mg & Pseudoephedrine HCl 120 mg Extended-Release Tablets, USP, 20 Extended-Release Tablets, Distributed by: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-7388-5.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed dissolution specifications
Published: December 15, 2021
Distribution: Nationwide

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FDA Recall Completed Historical recordClass I

AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA Vitamin E & Moisturizer, 8 FL OZ (237 mL) bottle with either a black or clear top, Distributed by American Screening LLC Shreveport, LA, 71106 UPC 8 40050 51579 2

by American Screening LLC

Reason: Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.
Published: December 15, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Mountain Meadow Herbs, Inc.

Product: Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3,…
Reason: Product bottle has potential to become pressurized over time. When consumer opens a bottle, the cap, capsules, and product powder could be forcefully expelled, and customers may sustain injuries to their hands and eyes.
Published: December 15, 2021
Distribution: distributed in IN, KY, MN, MO, MT, NE, N…

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FDA Recall United States Terminated Historical recordClass II

CONAGRA BRANDS

Product: Birds Eye Broccoli Tots, frozen, 12OZ bag UPC 00-0-14500-001…
Reason: Small rocks and metal fragments in the product
Published: December 15, 2021
Distribution: Nationwide

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FDA Recall Completed Historical recordClass I

Enoxaparin Sodium Injection, USP, 40 mg/0.4 mL, Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Rx Only; 0.4 mL Syringes, Manufactured for Sandoz Inc., Princeton, NJ 08540, NDC 00781-3246-02; Carton (10 x 0.4 mL Syringes), Manufactured by Shenzhen Techdow Pharmaceutical Co., Ltd. Shenzhen City, Guangdong Province 518057, China for Sandoz Inc., Princeton, NJ 08540, NDC 00781-3246-64

by Sandoz Inc

Reason: Temperature Abuse; temperature excursion during shipping
Published: December 8, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

5% Dextrose Injection, USP, 50 mL ADD-Vantage Unit, Rx only, Distributed by Hospira, INC., Lake Forest, IL 60045 USA, NDC 0409-7100-68/0409-7100-66

by Pfizer Inc.

Reason: Lack of sterility assurance: bag has the potential to leak.
Published: December 8, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Tydemy (drospirenone, ethinyl estradiol & levomefolate calcium tablets, 3 mg/0.03 mg/0.451 mg and levomefolate calcium tablets, 0.451 mg), packaged in cartons containing 3 wallets of 28 Tablets each, Rx Only, Distributed by: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, United Stated, Manufactured by: Lupin Limited, Pithampur, (M.P.) - 454775, India, 244896, The individual wallet NDC 68180-904-11 and the carton NDC 68180-904-13.

by Lupin Pharmaceuticals Inc.

Reason: Subpotent Drug
Published: December 8, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

KEURIG DR PEPPER

Product: Target Good & Gather Mixed Berry Sparkling Water 8 pack of 1…
Reason: The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained unlabeled sulfites.
Published: December 8, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

KEURIG DR PEPPER

Product: Target Good & Gather Coconut Pineapple Sparkling Water 8 pac…
Reason: The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained unlabeled sulfites.
Published: December 8, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

KEURIG DR PEPPER

Product: Polar Black Cherry Premium Seltzer 12 pack of 12oz cans UPC…
Reason: The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained unlabeled sulfites.
Published: December 8, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

KEURIG DR PEPPER

Product: 7UP Zero Sugar Lemon Lime Soda 12 pack of 12 oz. can UPC Car…
Reason: The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained unlabeled sulfites.
Published: December 8, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Onions 52

Product: 40# (LB) Ctn (box) Jumbo Yellow Onions, Product of Mexico -…
Reason: Voluntary recall due to possible contamination with Salmonella Oranienburg in onions from Chihuahua Mexico.
Published: December 8, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Onions 52

Product: 12 count per 2 lb. mesh sacks with UPC 033383 601014 Medium…
Reason: Voluntary recall due to possible contamination with Salmonella Oranienburg in onions from Chihuahua Mexico.
Published: December 8, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Onions 52

Product: 5# (LB) Ctn (box) Jumbo Red Onions, Product of Mexico - Labe…
Reason: Voluntary recall due to possible contamination with Salmonella Oranienburg in onions from Chihuahua Mexico.
Published: December 8, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Trail Toddy & Company LLC

Product: Spiced Irish Coffee Hint of Cocoa, each packet weighs 1.09 o…
Reason: Cream is declared in the Ingredients statement and Dairy is declared in the Contains statement. Milk is not declared.
Published: December 8, 2021
Distribution: distributed in Illinois and Montana, and…

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FDA Recall United States Terminated Historical recordClass II

Trail Toddy & Company LLC

Product: Mocha Irish Coffee 66% Cocao, each packet weighs 1.41 oz (40…
Reason: Cream is declared in the Ingredients statement and Dairy is declared in the Contains statement. Milk is not declared.
Published: December 8, 2021
Distribution: distributed in Illinois and Montana, and…

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FDA Recall United States Terminated Historical recordClass II

Trail Toddy & Company LLC

Product: Classic Irish Coffee Hint of Cocoa, each packet weighs 1.09…
Reason: Cream is declared in the Ingredients statement and Dairy is declared in the Contains statement. Milk is not declared.
Published: December 8, 2021
Distribution: distributed in Illinois and Montana, and…

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FDA Recall Terminated Historical recordClass III

Carvedilol Tablets, USP, 6.25 mg, 500 Tablets bottle, Rx Only, Distributed by: Aurobindo Pharma USA Inc., 279 Princeton-Hightstown Road, East Windsor, NJ, 08520, Made in India, NDC 65862-143-05

by Aurobindo Pharma USA Inc.

Reason: Failed Impurities/Degradation Specifications
Published: December 1, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Diclofenac Sodium Topical Solution USP, 1.5 w/w, 5 fl oz (150 mL) plastic bottles, Rx only, Teligent Pharma, Inc., Buena, New Jersey, 08310, NDC 70512-025-05.

by Teligent Pharma, Inc.

Reason: Defective Container
Published: December 1, 2021
Distribution: Nationwide

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Data last updated: September 16, 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.