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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.

37,113
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
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 5,921–5,940 of 18,555 recalls

FDA Recall Terminated Historical recordClass II

Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, Teligent Pharma Inc., Buena, NJ, 08310, NDC 52565-023-29

by Teligent Pharma, Inc.

Reason
Failed Stability Specifications: lot did not meet specification for the Active Pharmaceutical Ingredient (API) particle test, which was determined through routine stability testing
Published
January 5, 2022
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL), packaged in 50 mL screw cap bottles, Rx Only, Manufactured by Teligent Pharma, Inc., Buena, NJ 08310, Distributed by: McKesson Corporation dba Sky Packaging, 4971 Southridge Blvd., Suite 101, Memphis, TN 38141, NDC 63739-997-64

by Teligent Pharma, Inc.

Reason
Superpotent Drug: Minimally superpotent
Published
January 5, 2022
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL), packaged in 50 mL screw cap bottles, Rx Only, Manufactured by Teligent Pharma, Inc., Buena, NJ 08310, Distributed by: McKesson Corporation dba Sky Packaging, 4971 Southridge Blvd., Suite 101, Memphis, TN 38141, NDC 63739-997-64

by Teligent Pharma, Inc.

Reason
Superpotent Drug
Published
January 5, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Slayer Forever, LLC dba BUBS Naturals

Product
BUBS Naturals Fountain of Youth Formula; Collagen Protein; S…
Reason
Supplement contains undeclared milk from MCT oil powder ingredient.
Published
January 5, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Penicillin V Potassium for Oral Solution, USP 125 mg (200,000 U) per 5 mL a) 100 mL (NDC 00093-4125-73) and b) 200 mL (NDC 00093-4125-74) (when mixed) bottles, Rx Only, Manufactured For: Teva Pharmaceuticals USA, Inc. North Wales, PA 19454

by Teva Pharmaceuticals USA

Reason
Subpotent
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Rompe Pecho Max Multi-Symptoms Maximum Strength, 8 Fl. Oz. (237 mL) bottles, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166 UPC 0 00856 00309 5, NDC 58593-828-08

by Efficient Laboratories, Inc.

Reason
Microbial Contamination of Non-Sterile Products
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Rompe Pecho Ex Expectorant, packaged in a) 4 Fl. Oz. (118 mL) bottles NDC 58593-829-04 and b) 6 Fl. Oz. (178 mL) bottles NDC 58593-829-06, Distributed by Efficient Laboratories, Inc. Miami, FL 33166

by Efficient Laboratories, Inc.

Reason
Microbial Contamination of Non-Sterile Products
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Rompe Pecho DM, 6 Fl Oz (178 mL) bottles, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166, NDC 58593-275-06

by Efficient Laboratories, Inc.

Reason
Microbial Contamination of Non-Sterile Products
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Rompe Pecho CF Cold & Flu Advanced Formula, 6 Fl. oz. (178 mL) bottles, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166, NDC 58593-235-06

by Efficient Laboratories, Inc.

Reason
Microbial Contamination of Non-Sterile Products
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Fexofenadine Hydrochloride Tablets, 60 mg, 500 Tablets per bottle, Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152 NDC 0904-6979-40

by The Harvard Drug Group

Reason
Failed Impurities/Degradation Specifications
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Moxifloxacin, 1 mg/mL, 1mL in 2mL vial, solution for intracameral injection, 10 vials/carton, Rx only, Leiters 13796 Compark Blvd, Englewood, CO 80112, (800) 292-6772, NDC 71449-096-42

by Denver Solutions, LLC DBA Leiters Health

Reason
Labeling: Label Mix-up: Vials labeled as moxifloxacin 1 mg/mL may actually contain moxifloxacin 5 mg/mL
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Hand Sanitizer Foam (ethyl alcohol), 62% v/v, packaged in a) 1.5 Oz. cans, NDC 53329-970-12; b) 8 Oz. (227 g) cans, NDC 53329-970-08; and c) 16 Oz. (453 g) cans, NDC 53329-970-06; Manufactured for: Medline Industries, Inc., Northfield, IL 60093.

by Medline Industries Inc

Reason
Defective Container: Customer complaints for leaking bottles and dispensing issues.
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dakota Tom's, Inc

Product
Dakota Tom's and Market Fresh branded Chicken Salad Croissan…
Reason
Sandwiches contain undeclared egg and milk.
Published
December 29, 2021
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

GIVE AND GO

Product
Kimberley's bakeshoppe vanilla mini Frosted soft Sugar Cooki…
Reason
Potential for metal in product
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

GIVE AND GO

Product
Kimberley's bakeshoppe vanilla mini Frosted soft Sugar Cooki…
Reason
Potential for metal in product
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

GIVE AND GO

Product
Kimberley's bakeshoppe Frosted soft Sugar Cookies 13.5 oz. U…
Reason
Potential for metal in product
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

GIVE AND GO

Product
Favorite Day Bakery Frosted Sugar Cookies 13.5 oz. UPC 0 852…
Reason
Potential for metal in product
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

GIVE AND GO

Product
Wondershop at Target Frosted Sugar Cookies 13.5 oz. UPC 0 85…
Reason
Potential for metal in product
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

GIVE AND GO

Product
Favorite Day Bakery madeleine & brownie tiny treats 11 oz. U…
Reason
Potential for metal in product
Published
December 29, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

GIVE AND GO

Product
NL two-bite Cream Cheese Iced Cinnamon Roll 08030 16.93 lbs.…
Reason
Potential for metal in product
Published
December 29, 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.