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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.

37,142
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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
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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 11,721–11,740 of 19,943 recalls

FDA Recall United States Terminated Historical recordClass III

Smucker Natural Foods, Inc.

Product
SANTA CRUZ organic SEEDLESS RED RASPBERRY fruit spread NET W…
Reason
The firm was notified that the product did not have an ingredient panel or firm information on the label.
Published
April 25, 2018
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass III

Smucker Natural Foods, Inc.

Product
SANTA CRUZ organic MANGO fruit spread NET WT 9.5 OZ (270 g)…
Reason
The firm was notified that the product did not have an ingredient panel or firm information on the label.
Published
April 25, 2018
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass III

Smucker Natural Foods, Inc.

Product
SANTA CRUZ organic CONCORD GRAPE fruit spread NET WT 9.5 OZ…
Reason
The firm was notified that the product did not have an ingredient panel or firm information on the label.
Published
April 25, 2018
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass III

Smucker Natural Foods, Inc.

Product
SANTA CRUZ organic BLACKBERRY POMEGRANATE fruit spread NET W…
Reason
The firm was notified that the product did not have an ingredient panel or firm information on the label.
Published
April 25, 2018
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass III

Smucker Natural Foods, Inc.

Product
SANTA CRUZ organic APRICOT fruit spread NET WT 9.5 OZ (270 g…
Reason
The firm was notified that the product did not have an ingredient panel or firm information on the label.
Published
April 25, 2018
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Divinity Product Distribution LLC

Product
Kratom powder labeled in the following ways 1) Enhance Your…
Reason
The firm's dietary supplement products contain kratom (Mitragyna speciosa), a new dietary ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury;
Published
April 25, 2018
Distribution
Product distributed to the following US…

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FDA Recall United States Terminated Historical recordClass II

Divinity Product Distribution LLC

Product
Kratom capsules labeled in the following ways: 1) Divinity K…
Reason
The firm's dietary supplement products contain kratom (Mitragyna speciosa), a new dietary ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury;
Published
April 25, 2018
Distribution
Product distributed to the following US…

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FDA Recall Terminated Historical recordClass III

Decitabine for Injection, 50mg per vial, Rx only, Manufactured by: Cipla Ltd., Verna Goa, India, Manufactured for: Cipla USA, Inc., 1560 Sawgrass Corporate Parkway, Suite 130, Sunrise, FL 33323, NDC 69097-285-37

by InvaGen Pharmaceuticals, Inc.

Reason
Failed impurities/degradation specifications: Failure to water content and impurity
Published
April 18, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Zhong Hua Jiu (menthol 1%) Patch, Distributed by United Pacific Company, UPC 6 924938 100226, NDC 53614-001-02

by United Pacific Co Ltd

Reason
CGMP Deviations: the product was produced with substandard GMP manufacturing processes.
Published
April 18, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Conzerol (antipoxin) H2O2 Gel, Hydrogen Peroxide Gel 3%, 1.5 oz. tube, OTC, Manufactured for Elrose Labs, Inc., Sanford, FL

by Elroselabs Inc.

Reason
cGMP Deviations
Published
April 18, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Molleave, 2 oz bottle, OTC, Manufactured for Elrose Labs, Inc.

by Elroselabs Inc.

Reason
cGMP Deviations
Published
April 18, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Conzerol zero molluscum contagiosum, Topical Cream, Net weight 0.78 (22g), Elrose Labs, Sanford Fl 32771 USA --- NDC 70223-001-06

by Elroselabs Inc.

Reason
cGMP Deviations
Published
April 18, 2018
Distribution
Nationwide

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FDA Recall United States Completed Historical recordClass II

Poppies International INC

Product
GFS Belgian Mini Chocolate Topped Eclairs, Keep Frozen, Net…
Reason
Products may be contaminated with Listeria monocytogenes
Published
April 18, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Pepsi Cola Bottling Company

Product
Diet Pepsi; NOW ASPARTAME FREE; 6 PACK; 16 OZ BOTTLES; 6-16…
Reason
Case labeling (shrink-wrap labeling) for Diet Pepsi 6 packs (6-16oz bottles) may indicate that the product is "Now Aspartame Free" when the product actually contains aspartame. The individual 16 oz. bottles have aspartame declared in the ingredient statements. The outer wrapping has the incorrect/misdeclared "Now Aspartame Free" declaration.
Published
April 18, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Bestco, Inc.

Product
Signature Care Calcium Chews; Dietary Supplement; 500 mg Cal…
Reason
A packaging revision and lack of revision to the corresponding packaging batch record caused the labeling for the firm's Signature Care brand Calcium Chews dietary supplement to declare a higher level of Vitamin D than the product actually contained. The bag declares 25 mcg (1000 IU) of Vitamin D. The product actually contains 12.5 mcg (500 IU) of Vitamin D.
Published
April 18, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

All American Seasonings, Inc.

Product
LOST CAJUN GUMBO BASE, T4014, PACK SIZE 45 lb bag, Blended b…
Reason
All American Seasonings is recalling Lost Cajun Gumbo Base because an ingredient was contaminated with Salmonella.
Published
April 18, 2018
Distribution
One customer in Colorado.

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FDA Recall Terminated Historical recordClass III

buPROPion HCl Extended-Release Tablets, USP (SR), 150 mg ,a) 60 count (NDC 69097-878-03) and b) 100 count (NDC 69097-878-07) bottles, Rx Only, Manufactured for: Cipla USA Inc. 1560 Sawgrass Corporate Parkway Suite 130 Sunrise, FL 33323, Manufactured by: InvaGen Pharmaceuticals, Inc. (a subsidiary of Cipla Ltd.) Hauppauge, NY 11788

by InvaGen Pharmaceuticals, Inc.

Reason
Failed Dissolution Specifications; during stability testing
Published
April 11, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

buPROPion HCl Extended-Release Tablets, USP (SR), 100 mg, 60 count bottles, Rx Only, Manufactured for: Cipla USA Inc. 1560 Sawgrass Corporate Parkway Suite 130 Sunrise, FL 33323, Manufactured by: InvaGen Pharmaceuticals, Inc. (a subsidiary of Cipla Ltd.) Hauppauge, NY 11788 --- NDC 69097-877-03

by InvaGen Pharmaceuticals, Inc.

Reason
Failed Dissolution Specifications; during stability testing
Published
April 11, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Fabior (tazarotene) Foam, 0.1%, 100 grams can, Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834; NDC 51862-295-10.

by Mayne Pharma Inc

Reason
Superpotent Drug: High out of specification results for tazarotene assay at the 9-month stability time point.
Published
April 11, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Pepsi Beverage Co

Product
diet Pepsi, 12 FL OZ, in aluminum cans packaged in 12 pk pap…
Reason
Diet Pepsi product is labeled to contain the artificial sweetener Sucralose, but actually contains Aspartame
Published
April 11, 2018
Distribution
Distributed for sale in hotels in CO, LA…

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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.