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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,116
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/saratoga-potato-chips-issues-allergy-alert-undeclared-soy-j-higgs-loaded-bacon-and-cheddar-potatoPublished September 16, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 6,821–6,840 of 20,288 recalls

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

View recall →

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

View recall →

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

View recall →

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

View recall →

FDA Recall United States Terminated Historical recordClass II

Flowers Foods (Corporate Offices)

Product
Tastykake Jelly Krimpets 12oz (6-2ct) UPC 0 25600 00228 5 &…
Reason
The firm was notified by an ingredient supplier of the potential small metal fragments in one of the ingredients.
Published
December 8, 2021
Distribution
Products was distributed to the followin…

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FDA Recall United States Terminated Historical recordClass II

Flowers Foods (Corporate Offices)

Product
Tastykake Creme Filled Krimpets 14.25oz (6-2ct) UPC 0 25600…
Reason
The firm was notified by an ingredient supplier of the potential small metal fragments in one of the ingredients.
Published
December 8, 2021
Distribution
Products was distributed to the followin…

View recall →

FDA Recall United States Terminated Historical recordClass II

Flowers Foods (Corporate Offices)

Product
Tastykake Butterscotch Krimpets 24oz (12-2ct) UPC 0 25600 00…
Reason
The firm was notified by an ingredient supplier of the potential small metal fragments in one of the ingredients.
Published
December 8, 2021
Distribution
Products was distributed to the followin…

View recall →

FDA Recall United States Terminated Historical recordClass II

Flowers Foods (Corporate Offices)

Product
Tastykake Chocolate Creme Filled Cupcakes 14.25oz, UPC 0 256…
Reason
The firm was notified by an ingredient supplier of the potential small metal fragments in one of the ingredients.
Published
December 8, 2021
Distribution
Products was distributed to the followin…

View recall →

FDA Recall United States Terminated Historical recordClass II

Flowers Foods (Corporate Offices)

Product
Tastykake Chocolate Cupcakes 12.75oz, UPC 0 25600 00219 3
Reason
The firm was notified by an ingredient supplier of the potential small metal fragments in one of the ingredients.
Published
December 8, 2021
Distribution
Products was distributed to the followin…

View recall →

FDA Recall United States Terminated Historical recordClass II

Flowers Foods (Corporate Offices)

Product
Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes 1…
Reason
The firm was notified by an ingredient supplier of the potential small metal fragments in one of the ingredients.
Published
December 8, 2021
Distribution
Products was distributed to the followin…

View recall →

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

View recall →

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

View recall →

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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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 52565-002-05

by Teligent Pharma, Inc.

Reason
Defective Container
Published
December 1, 2021
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass III

Butalbital, APAP, Caf 50/325/40 Tablet, packaged in a) 12-count bottles, NDC: 71335-1767-09, barcode 083929164865; b) 20-count bottles, NDC: 71335-1767-01, barcode 083921157837; c) 30-count bottles, NDC: 71335-1767-02, barcode 083922165687, d) 60-count bottles, NDC: 71335-1767-03, barcode 083923153776, e) 90-count bottles, NDC: 71335-1767-04, barcode 083924152889, f) 120-count bottles, NDC: 71335-1767-07, barcode 083927153735. Westminster Pharmaceuticals LLC, Rx only, Packaged by Bryant Ranch Prepack, Burbank, CA 91504 USA

by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Reason
Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label
Published
December 1, 2021
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Butalbital, APAP, Caf 50/325/40 Tablets, packaged in a) 12-count bottles, NDC: 63629-8392-09, barcode 083929152151; b) 60-count bottles, NDC: 63629-8392-03, barcode 083923152614; c) 90-count bottles, NDC:63629-8392-04, barcode 083924152614, Lannett Company Inc; Rx only, Packaged by Bryant Ranch Prepack, Burbank, CA 91504.

by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Reason
Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label
Published
December 1, 2021
Distribution
Nationwide

View recall →

Data last updated:

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.