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Recall totals

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

37,066

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 14, 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 Terminated Historical recordClass III

12 HR Allergy & Congestion Relief Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg Antihistamine I Nasal Decongestant, 20 Extended-Release Tablets USP, Distributed By Cardinal Health, Dublin, Ohio 43107, Made in India, NDC 70000-0518-1.

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

Antihistamine & Nasal Decongestant, Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg, Extended Release Tablets USP, Allergy & Congestion, 12 Hour, 30 Tablets, Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152, www.rugbylaboratories.com. NDC 0638-1242-07.

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

Antihistamine & Nasal Decongestant, Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg, Extended Release Tablets USP, Allergy & Congestion, 12 Hour, 20 Tablets, Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152, www.rugbylaboratories.com. NDC 0536-1242-34.

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

Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Tablets USP Allergy & Congestion, 20 Tablets, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, NDC 43598-823-14.

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 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

Cargill Cocoa & Chocolate, Inc.

Product: Wilbur Dark Chocolate Triple Covered Malted Milk Balls, 1-po…
Reason: Product recalled because of the presence of undeclared peanuts.
Published: December 15, 2021
Distribution: The product was distributed in the State…

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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 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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Data last updated: September 14, 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.