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

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Source: FDA and USDA public dataLast updated September 15, 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 United States Terminated Historical recordClass II

KRAFT HEINZ FOODS COMPANY

Product: Country Time Original Lemonade drink mix powder 2.4 KG UPC…
Reason: potential for glass and metal in product
Published: December 22, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

KRAFT HEINZ FOODS COMPANY

Product: Country Time Lemonade drink mix powder 19 oz. UPC 04300095…
Reason: potential for glass and metal in product
Published: December 22, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

KRAFT HEINZ FOODS COMPANY

Product: Country Time Pink Lemonade powder drink mix 19 oz. UPC 04…
Reason: potential for glass and metal in product
Published: December 22, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

KRAFT HEINZ FOODS COMPANY

Product: Kool-Aid Tropical Punch powder drink mix 19 oz. UPC 043000…
Reason: potential for glass and metal in product
Published: December 22, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

RIPPLE FOODS PBC

Product: Ripple Dairy-Free. As It Should Be 8g Plant Based Protein; H…
Reason: Complaint led investigation found the presence of Bacillus Cereus in one lot of product.
Published: December 22, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325 mg, 100-count bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc., Central Islip, NY 11722, NDC 31722-997-01.

by Ascent Pharmaceuticals, Inc.

Reason: Product Mix-up
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 and Congestion, 30 Tablets, Distributed by: Dr. Reddy's Laboratories, Inc., Princeton, NJ, 08640, Made in India NDC Walmart Inc., Bentonville, AR 72716, Product of India, NDC 43598-823-31.

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 Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, USP, 30 Extended-Release Tablets USP, Distributed By Walmart Inc., Bentonville, AR 72716, Product of India, NDC 49035-273-30.

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 Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, 30 Extended-Release Tablets USP, Distributed By CVS Pharmacy Inc., One CVS Drive, Woonsocket, RI 02985, Made in India, NDC 69842-249-30

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

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 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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Data last updated: September 15, 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.