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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 October 2026.

37,324
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,859
Class I recallsReasonable probability of serious health consequences
24,440
Class II recallsTemporary or medically reversible health consequences
2,900
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 2,095 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,440
Class I9,859
Class III2,900
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,440
Class I9,859
Class III2,900
Not Yet Classified2

Showing 4,941–4,960 of 17,324 recalls

FDA Recall TerminatedTerminated: June 17, 2024Historical recordClass II

Clobetasol Propionate Lotion, 0.05%, packaged in a) 2 fl. oz. (59 mL) bottles, NDC 52565-055-02; b) 4 fl. oz. (118 mL) bottles, NDC 52565-055-04, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: June 17, 2024Historical recordClass II

Clobetasol Propionate Cream USP, 0.05% (Emollient), packaged in a) 15 grams tube, NDC 52565-094-15; b) 30 grams tube, NDC 52565-094-30; c) 45 grams tube, NDC 52565-094-45; d) 60 grams tube, NDC 52565-094-60, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: June 17, 2024Historical recordClass II

Clobetasol Propionate Cream USP, 0.05%, packaged in a) 15 grams tube, NDC 52565-051-15; b) 30 grams tube, NDC 52565-051-30; c) 45 grams tube, NDC 52565-051-45; d) 60 grams tube, NDC 52565-051-60; Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: June 17, 2024Historical recordClass II

Betamethasone Dipropionate Lotion USP, 0.05%* (Augmented), packaged in a) 30 mL (29 grams) bottles, NDC 52565-023-29; b) 60 mL (58 grams) bottles, NDC 52565-023-59, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: August 1, 2022Historical 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 TerminatedTerminated: December 2, 2022Historical 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 TerminatedTerminated: March 16, 2023Historical 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 TerminatedTerminated: July 16, 2023Historical 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 TerminatedTerminated: July 6, 2022Historical 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 TerminatedTerminated: December 9, 2022Historical 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 TerminatedTerminated: June 24, 2022Historical 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 TerminatedTerminated: June 24, 2022Historical 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 TerminatedTerminated: April 15, 2022Historical 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 TerminatedTerminated: July 16, 2023Historical 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 TerminatedTerminated: June 8, 2023Historical 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 OngoingHistorical 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 OngoingHistorical 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

View recall →

FDA Recall United States OngoingHistorical 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 →

FDA Recall United States OngoingHistorical recordClass I

Abbott Laboratories

Product
Abbott Similac Organic with A2 Milk Infant Formula with Iron…
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 →

FDA Recall United States OngoingHistorical recordClass I

Abbott Laboratories

Product
Abbott Similac Pro-Advance Infant Formula with Iron 20.6oz.…
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.

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