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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 3,761–3,780 of 17,993 recalls

FDA Recall Terminated Historical recordClass II

Maximum Zone2 Topical Analgesic, 1oz bottle, for use during a pain sensitive procedure, distributed by: DERMAL SOURCE, Portland, OR, www.dermalsource.com, 1-866-568-3223, NDC code: 80069-012-01, Drug Facts- For use by licensed professionals only' Active Ingredients- Lidocaine HCL (5%), Epinephrine (0.01%).

by HTO Nevada, Inc.

Reason
cGMP Deviation: Raw material recalled by repackager, due to discoloration of the epinephrine API.
Published
February 22, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

New & Improved Blue Gel Anesthetic, to reduce pain and swelling during pain sensitive procedures, 1 oz bottle, distributed by Dermal Source, Portland, OR, www.dermalsource.com 1-888-568-3223. NDC Code: 80069-008-01. Drug Facts- For use by licensed professionals only, Active Ingredients -Lidocaine HCL (5%), Tetracaine HCL (1%) and epinephrine (0.1%).

by HTO Nevada, Inc.

Reason
cGMP Deviation: Raw material recalled by repackager, due to discoloration of the epinephrine API.
Published
February 22, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, packaged in (a) 100-count bottle, NDC 68001-501-00; (b) 500-count bottle, NDC 68001-501-03. Manufactured by Alkem Laboratories Ltd., India. For BluePoint Laboratories

by Amerisource Health Services LLC

Reason
Failed Dissolution Specifications: This recall is being initiated in support of the recall by the manufacturer which included lots that were packaged for BluePoint Laboratories.
Published
February 22, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Thiamine Hydrochloride 3000 mg/30 mL (100mg/mL), Riboflavin 30 mg/30 mL (1mg/mL) Injection, FOR INTRAMUSCULAR OR SLOW INTRAVENOUS USE, 30 mL Sterile Multiple Use Vial, Rx Only, Compounded for a licensed professional or patient use by: McGuff Compounding Pharmacy Services, Inc, Santa Ana, CA 92704.

by McGuff Compounding Pharmacy Services, Inc.

Reason
Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.
Published
February 22, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Thiamine Hydrochloride 200 mg/2mL (100mg/mL), Riboflavin 2 mg/2mL (1mg/mL) Injection, FOR INTRAMUSCULAR OR SLOW INTRAVENOUS USE, 2 mL Sterile Single Use Vial, Preservative-Free, Rx Only, Compounded for a licensed professional or patient use by: McGuff Compounding Pharmacy Services, Inc, Santa Ana, CA 92704.

by McGuff Compounding Pharmacy Services, Inc.

Reason
Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.
Published
February 22, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pepsico Inc

Product
Starbucks frappuccino Vanilla. Chilled Coffee Drink. 13.7 F…
Reason
Foreign object (glass).
Published
February 22, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Posaconazole Delayed-Release Tablets, 100 mg, 60-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ 08830-3009; Manufactured by: Biocon Pharma Limited, Bengaluru, India - 560 099, NDC 70377-038-11.

by BIOCON PHARMA INC

Reason
Failed Impurities/Degradation Specifications: High Out Of Specification degradation results.
Published
February 15, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Atropine Sulfate Ophthalmic Solution, USP 1%, For Topical Application To The Eye, 2 mL bottle, Sterile, Rx only, Distributed by: Akorn Operating Company LLC, Gurnee, IL 60031. NDC: 17478-215-02

by Akorn, Inc.

Reason
Failed Stability Specifications: Out of specification test results for viscosity was identified at the 12M stability timepoint.
Published
February 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v, 8 FL OZ (237 ML) bottles.

by Urban Electric Power

Reason
CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Published
February 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ohm Hand Sanitizer (alcohol (ethanol) 70 % v/v), packaged in a) 2 FL OZ (60 ML), b) 3 FL OZ (88 ML) bottles, c) 10 FL OZ (295 ML) bottles, d)12 FL OZ (355 ML) bottles, e)16 FL OZ (473 ML) bottles, f) 64 FL OZ (1892 ML) bottles, g) 128 FL OZ (3785 ML) bottles

by Urban Electric Power

Reason
CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Published
February 15, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Mondelez Global Llc

Product
Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) UP…
Reason
Undeclared FD&C Yellow No. 5
Published
February 15, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ortho Molecular Products, Inc.

Product
Fiber Powder, Dietary Supplement, Apple Cinnamon Flavored, p…
Reason
Raw material tested positive for Cronobacter sakazakii.
Published
February 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Diltiazem Hydrochloride Extended-Release Capsules, USP, 360 mg; Rx only; 90-count bottles, Manufactured by: Sun Pharmaceutical Industries Ltd. Halol-Baroda Highway, Halol-389350, Gujarat, India; Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, NDC 47335-679-81

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Impurity (Deacetyl Diltiazem Hydrochloride) specification during stability testing and failed dissolution testing at FDA laboratory.
Published
February 8, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Global Care 70% Alcohol Ethyl Rubbing Alcohol, packaged in a) 32 FL OZ (946 mL) UPC 8 70373 01323 1; b) 16 FL OZ (473 mL) UPC 8 70373 01332 3; c) 1 Gallon (128 FL OZ) 3785.41 mL UPC 8 70373 01330 4, Dist. By Target Price, Inc. Catano, PR

by Frenda Corporation

Reason
cGMP Deviations
Published
February 8, 2023
Distribution
Puerto Rico

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FDA Recall Terminated Historical recordClass II

Global Care Antibacterial Hand Sanitizer Alcohol Etilico 70% Original, 1 Gallon (128 FL OZ) 3785.41 mL, Dist. by Target Price, Inc. Catano, PR, UPC 8 70373 01326 2

by Frenda Corporation

Reason
cGMP Deviations
Published
February 8, 2023
Distribution
Puerto Rico

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FDA Recall Terminated Historical recordClass II

Easy Clean 75% Ethyl Alcohol, packaged in a) 1 Gallon (128 fl. oz.) UPC 8 91857 00045 5; b) 16 fl. oz. (473 mL) UPC 8 91857 00055 4; c) Rubbing Alcohol 10 fl. oz. (296 mL) UPC 8 91857 00044 8, Manufactured by Frenda Corporation Trujillo Alto, PR 00976

by Frenda Corporation

Reason
cGMP Deviations
Published
February 8, 2023
Distribution
Puerto Rico

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FDA Recall Terminated Historical recordClass II

Easy Clean 70% Isopropyl Alcohol, packaged in a) 1 Gallon (128 fl. oz.) UPC 8 91857 00048 6; b) 16 fl. oz. (473 mL) UPC 8 91857 00047 9, Manufactured by: Frenda Corporation Trujillo Alto, PR 00976

by Frenda Corporation

Reason
cGMP Deviations
Published
February 8, 2023
Distribution
Puerto Rico

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FDA Recall Terminated Historical recordClass II

Easy Clean Isopropyl Alcohol 99%, 1 Gallon (128 fl. oz.), Manufactured by: Frenda Corporation Trujillo Alto, PR 00976, UPC 8 91857 00054 7

by Frenda Corporation

Reason
cGMP Deviations
Published
February 8, 2023
Distribution
Puerto Rico

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FDA Recall Terminated Historical recordClass II

Easy Clean Alcohol Mult Surface Disinfecting Cleaner 75% Ethyl Alcohol, 32 FL. OZ. (946 mL.), Manufactured by: Frenda Corporation Trujilio Alto, PR 00976, UPC 8 91857 00052 3

by Frenda Corporation

Reason
cGMP Deviations
Published
February 8, 2023
Distribution
Puerto Rico

View recall →

FDA Recall Terminated Historical recordClass II

Easy Clean Antiseptic Hand Sanitizer Solution 65% with Glycerine, 1 Gallon (128 Fl. oz.), Manufactured by: Frenda Corporation Trujillo Alto, PR 00976, UPC 8 91857 00050 9

by Frenda Corporation

Reason
cGMP Deviations
Published
February 8, 2023
Distribution
Puerto Rico

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.