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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 6,941–6,960 of 21,626 recalls

FDA Recall Terminated Historical recordClass I

REVITADERM WOUND CARE GEL, (Benzalkonium Chloride in a gel containing transforming growth factor-b), 0.1%, packaged in 29.6 mL (1.0 FL OZ) bottles (NDC 63347-120-02) and 88.7 mL (3.0 FL OZ) tubes (NDC 63347-120-01), Blaine Labs Inc., Santa Fe Springs, CA 90670

by Blaine Labs Inc

Reason
Microbial Contamination of Non-sterile Product; FDA analysis found the product to be contaminated with Bacillus cereus.
Published
March 30, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Flow Beverages Inc.

Product
Flow Alkaline Spring Water - Organic lemon & ginger flavored…
Reason
Flow Beverages Inc., 33 Lakeview CT., Verona, VA, 24482 is initiating a recall of Flow Alkaline Spring Water - Organic lemon & ginger flavored water, 500 ml 12 units per case, Lots 2023AUG29 V5 and 2023AUG29 V5 because of four (4) customer complaints of alleged adverse reactions following the consumption of Flow organic lemon + ginger flavored water, 16.9 fl oz. (500 ml),
Published
March 30, 2022
Distribution
The product was distributed to the follo…

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FDA Recall United States Terminated Historical recordClass II

Flow Beverages Inc.

Product
Flow Alkaline Spring Water - Organic lemon & ginger flavored…
Reason
Flow Beverages Inc., 33 Lakeview CT., Verona, VA, 24482 is initiating a recall of Flow Alkaline Spring Water - Organic lemon & ginger flavored water, 500 ml 12 units per case, Lots 2023AUG29 V5 and 2023AUG29 V5 because of four (4) customer complaints of alleged adverse reactions following the consumption of Flow organic lemon + ginger flavored water, 16.9 fl oz. (500 ml),
Published
March 30, 2022
Distribution
The product was distributed to the follo…

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FDA Recall Terminated Historical recordClass I

Avaphinal Maximum Male Enhancement Sexual Pills, 2000 MG*, packaged in 10 Capsules per carton.

by Walmart Stores

Reason
Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published
March 23, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

0.9% Sodium Chloride Injection USP, 250 mL Excel Container, Rx only, B. Braun Medical Inc., Bethlehem, PA, NDC 0264-7800-20

by B. Braun Medical, Inc.

Reason
Lack of sterility assurance: leaking bags
Published
March 23, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

hydrALAZINE HCl Tablets, USP, 10 mg, 100 Tablets per carton (10x10 blister packs), Rx only, Distributed by: MAJOR PHARMACEUTICALS, Livonia, MI 48152 USA. NDC # 0904-6440-61

by The Harvard Drug Group

Reason
Failed Impurities/Degradation Specifications: Out of specification result obtained during routine stability testing for Impurities.
Published
March 23, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

FDMR, INC DBA SUJI'S KOREAN CUISINE

Product
Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a…
Reason
Hazelnuts were declared in ingredient statement but not in Contains statement.
Published
March 23, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

RON DAVIES JR

Product
Bob Evan's Sour Cream & Chive Mashed Potatoes 24oz plastic…
Reason
Incorrect packaging for product resulting in an undeclared wheat allergen
Published
March 23, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Swanson Health Products, Inc

Product
Swanson Ultra: Vitamin B12 Methylcobalamin High Absorption…
Reason
Dietary supplement may contain potential metal shavings greater than or equal to 7mm in length.
Published
March 23, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Gourmet Kitchen, Inc.

Product
14" Raw Buttermilk Breakfast Tart with Fresh Blueberries &…
Reason
Undeclared almonds
Published
March 23, 2022
Distribution
Distributed to 4 distributors and 21 dir…

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FDA Recall United States Terminated Historical recordClass I

Gourmet Kitchen, Inc.

Product
14" Raw Buttermilk Breakfast Tart with Cranberries, Apples &…
Reason
Undeclared almonds
Published
March 23, 2022
Distribution
Distributed to 4 distributors and 21 dir…

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FDA Recall United States Terminated Historical recordClass I

The Royal Ice Cream Company Inc.

Product
All Ice Cream and Ice Cream products within expiry; manufact…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
March 23, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Mohammad Mayha

Product
Helmi Honey VIP packaged in a gold paper box with black writ…
Reason
Contains hidden drug ingredient
Published
March 23, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Mohammad Mayha

Product
Jaguar Power Honey packaged in a gold paper box with black w…
Reason
Contains hidden drug ingredient
Published
March 23, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Herbalife International of America

Product
Herbalife NutritionProtein Bar Deluxe - Chocolate Peanut fla…
Reason
Undeclared allergen - egg
Published
March 23, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Oxycodone Hydrochloride Oral Solution, USP (C-II), 5 mg/5 mL, Delivers 5 mL per Cup, 1 Tray of 10 Cups, Rx Only, For Institutional Use Only, American Health Packaging, Columbus, OH 43217. UPC (01) 003 60687 406 40 4; Case NDC#: 60687-406-77, Unit Dose NDC#: 60687-406-40

by American Health Packaging

Reason
Impurity failure at 0-time of the repackaged lot.
Published
March 16, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PALIPERIDONE EXTENDED-RELEASE TABLETS, 9 mg, 100 Tablets per carton (10 x 10 blister packs), Rx only, Manufactured by: Sun Pharmaceutical Industries Ltd., Survey No. 259/15, Dadra-396 191, India. Distributed by: MAJOR PHARMACEUTICALS, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152. NDC: 0904-6937-61

by The Harvard Drug Group

Reason
Failed Dissolution Specifications
Published
March 16, 2022
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass I

Abbott Laboratories

Product
Abbott Similac PM 60/40 Low Iron Infant Formula, 14.1oz. can…
Reason
Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
Published
March 16, 2022
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass I

Abbott Laboratories

Product
Abbott Infant Formula Powder 12.6oz. can. 6 cans per case.…
Reason
Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
Published
March 16, 2022
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass I

Abbott Laboratories

Product
Abbott EleCare Jr Amino Acid-Based Nutrition Powder Unflavor…
Reason
Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
Published
March 16, 2022
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.