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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.

37,115
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

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 7,281–7,300 of 18,374 recalls

FDA Recall Terminated Historical recordClass III

Potassium Chloride Extended-Release Tablets USP, 10mEq (750mg), 1000-count bottle, Rx only, Manufactured by: Strides Shasun Limited Bengaluru - 562106, India, Distributed by: Strides Pharma Inc., East Brunswick, NJ 08816, NDC 64380-861-08

by Strides Pharma Science Limited

Reason
Failed Tablet/Capsules Specifications: Oversized tablets were found in one lot of Potassium Chloride Tablets 750 mg.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 200 tablets per bottle. [Brand, NDC] NDC Basic Care: 0113-7852-82; NDC CVS Health: 59779-540-82; NDC HEB: 37808-507-82; NDC Signature Care: 21130-116-82; NDC Walgreens: 0363-0852-82

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets, USP 150 mg, 95 tablets per bottle. [Brand, NDC] NDC Basic Care: 0113-7950-01; NDC CVS Health: 59779-950-01

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 90 tablets per bottle. [Brand, NDC] NDC Equate: 49035-608-75; NDC Up & Up: 11673-023-75

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 65 tablets per bottle. [Brand, NDC] NDC Care One: 41520-392-09; NDC CVS Health: 59779-540-09; NDC Family Wellness: 55319-852-09; NDC Good Neighbor Pharmacy: 46122-532-09; NDC HEB: 37808-507-09; NDC Health Mart: 49348-109-54; NDC Meijer: 41250-891-09; NDC Rite Aid: 11822-0852-3; NDC Shopko: 37012-852-09; NDC Sound Body: 50594-852-09; NDC Sunmark: 49348-109-54; NDC Up & Up: 11673-852-09; NDC Walgreens: 0363-0852-09

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 50 tablets per bottle. [Brand, NDC] NDC DG Health: 55910-852-71; NDC Good Neighbor Pharmacy: 46122-224-71; NDC Good Sense: 0113-0852-71; NDC Harris Teeter: 69256-041-71; NDC Kroger: 30142-600-71; NDC Major: 0904-6716-51; NDC Meijer: 41250-852-71; NDC Publix: 56062-099-71; NDC Rite Aid: 11822-0852-2; NDC Signature Care: 21130-116-71; NDC Topcare: 36800-852-71

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets, USP 150 mg, 40 tablets per bottle. [Brand, NDC] NDC Up & Up: 11673-950-58

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets, USP 150 mg, 24 tablets per bottle. [Brand, NDC] NDC Care One: 41520-609-62; NDC CVS Health: 59779-950-62; NDC DG Health: 55910-423-62; NDC Equaline: 41163-950-62; NDC Family Wellness: 55319-523-62; NDC Good Neighbor Pharmacy: 46122-041-62; NDC HEB: 37808-710-02; NDC Kroger: 30142-891-02; NDC Leader: 70000-0378-1; NDC Meijer: 41250-950-02; NDC Rite Aid: 11822-0950-0; NDC Shopko: 37012-950-62; NDC Signature Care: 21130-568-62; NDC Topcare: 36800-950-62; NDC Walgreens: 0363-0950-02

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 24 tablets per bottle. [Brand, NDC] NDC Being Well: 46994-852-62; NDC Care One 41520-392-02; NDC CVS Health: 59779-540-02; NDC DG Health: 55910-852-02; NDC Equaline: 41163-852-62; NDC Equate: 49035-608-02; NDC Exchange Select: 55301-852-02; NDC Family Wellness: 55319-852-02; NDC Good Neighbor Pharmacy: 46122-224-62; NDC Good Sense 0113-0852-62; NDC Harris Teeter: 69256-041-62; NDC Health Mart 49348-109-04; NDC Kroger 30142-600-02; NDC Major 0904-6716-24; NDC Meijer: 41250-852-02; NDC Publix: 56062-099-02; NDC Rite Aid 11822-0852-5; NDC Select 7: 10202-852-62; NDC Shop Rite 41190-852-62; NDC Shopko: 37012-852-62; NDC Signature Care: 21130-116-02; NDC Sound Body: 50594-852-02; NDC Sunmark: 62011-0282-1; NDC Topcare: 36800-852-02; NDC Up & Up: 11673-023-02; NDC Walgreens: 0363-0852-62

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 160 tablets per bottle. [NDC: Brand] NDC CVS Health.: 69842-293-06

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 80 tablets per bottle. [NDC: Brand] NDC Basic Care: 0113-7876-27; NDC CVS Health: 69842-293-27; NDC Leader: 70000-0375-2; NDC Up & Up: 11673-876-27; NDC Walgreens: 0363-1876-27

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 30 tablets per bottle. [NDC: Brand] NDC CVS Health: 69842-293-65; NDC Equaline 41163-931-65; NDC Family Wellness: 55319-876-65; NDC Good Sense 0113-0876-65; NDC H.E.B.: 37808-876-65; NDC Harris Teeter: 69256-876-65; NDC Health Mart: 62011-0283-1; NDC Leader: 62011-0283-1; NDC Major: 0904-6715-46; NDC Signature Care: 21130-118-65; NDC Sunmark: 49348-136-44; NDC Up & Up: 11673-876-65; NDC Walgreens: 0363-1876-65

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Chicago Indoor Garden, Inc.

Product
Mixed Greens 4 oz. Product contains red clover sprouts.
Reason
FDA sample analysis of sprouts was positive for E. coli. FDA traceback and epi associate the firms sprouts with an outbreak of E. coli.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Chicago Indoor Garden, Inc.

Product
Sprout Salad 6 oz. Product contains red clover sprouts.
Reason
FDA sample analysis of sprouts was positive for E. coli. FDA traceback and epi associate the firms sprouts with an outbreak of E. coli.
Published
March 25, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Chicago Indoor Garden, Inc.

Product
Spring Salad 6 oz. Product contains red clover sprouts.
Reason
FDA sample analysis of sprouts was positive for E. coli. FDA traceback and epi associate the firms sprouts with an outbreak of E. coli.
Published
March 25, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Chicago Indoor Garden, Inc.

Product
Red Clover 4 oz, Red Clover 2 Lbs. Products have Red Clover…
Reason
FDA sample analysis of sprouts was positive for E. coli. FDA traceback and epi associate the firm's sprouts with an outbreak of E. coli.
Published
March 25, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Moonstruck Chocolate Company

Product
Moonstruck Praline Pecan & Ginger Element Bar in Dark Chocol…
Reason
Undeclared milk.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Dreyers Grand Ice Cream, Inc.

Product
Outshine Fruit Bars - Variety Pack (contains 24 x 5 oz. unit…
Reason
Firm has received consumer complaints of pieces of white plastic in frozen fruit bars.
Published
March 25, 2020
Distribution
AL, AR, AZ, CA, CO, CT, DE, FL, GA, IL,…

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FDA Recall United States Terminated Historical recordClass II

Dreyers Grand Ice Cream, Inc.

Product
Outshine Fruit Bars Pineapple; 6 Fruit Ice Bars; 6x2 5 fl.…
Reason
Firm has received consumer complaints of pieces of white plastic in frozen fruit bars.
Published
March 25, 2020
Distribution
AL, AR, AZ, CA, CO, CT, DE, FL, GA, IL,…

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FDA Recall United States Terminated Historical recordClass II

Dreyers Grand Ice Cream, Inc.

Product
Outshine Fruit Bars Strawberry; 6 Fruit Ice Bars; 14.7 Fl.…
Reason
Firm has received consumer complaints of pieces of white plastic in frozen fruit bars.
Published
March 25, 2020
Distribution
AL, AR, AZ, CA, CO, CT, DE, FL, GA, IL,…

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.