Skip to main content
Get Alerts

Data Explorer

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.

37,341
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,860
Class I recallsReasonable probability of serious health consequences
24,450
Class II recallsTemporary or medically reversible health consequences
2,901
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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/haifa-smoked-fish-recalls-cold-smoked-sprats-due-potential-health-riskPublished October 27, 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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

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 II24,450
Class I9,860
Class III2,901
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,450
Class I9,860
Class III2,901
Not Yet Classified2

Showing 1,981–2,000 of 25,393 recalls

FDA Recall United States TerminatedTerminated: July 1, 2025Historical recordClass I

TRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE SEA FROZEN FOOD

Product
Frozen Shrimp- packaged in 5lb frozen IQF blocks/4 blocks to…
Reason
Frozen Raw Peeled & Deveined tail on, shrimp contains undeclared sulfites
Published
July 2, 2025
Distribution
Affected lots were sold exclusively to W…

View recall →

FDA Recall United States TerminatedTerminated: April 28, 2026Historical recordClass III

MORTON SALT INC

Product
Windsor brand Extra Course Sea Salt Grinder Refill, 255 g, p…
Reason
The quantity of product in each unit does not match the stated weight.
Published
July 2, 2025
Distribution
All product exported for sale in Canada…

View recall →

FDA Recall CompletedHistorical recordClass I

UMOVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7503046054134

by Umary-USA.com

Reason
Marketed without approved NDA/ANDA- Laboratory analysis found product to be tainted with undeclared ingredients: Dexamethasone and Diclofenac.
Published
June 25, 2025
Distribution
Nationwide

View recall →

FDA Recall CompletedHistorical recordClass I

UNAVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7 503046 054295

by Umary-USA.com

Reason
Marketed without approved NDA/ANDA- Laboratory analysis found product to be tainted with undeclared ingredients: Dexamethasone, Diclofenac and Omeprazole.
Published
June 25, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Gentamicin Injection, USP, (PEDIATRIC), 20 mg per 2 mL (10 mg per mL*), 2 mL Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ, 08520 Vial- NDC 55150-401-01, Carton NDC 55150-401-25

by Eugia US LLC

Reason
Failed Stability Specifications: Out of specification results for the Color Absorbance test during 12 Month sample analysis.
Published
June 25, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Acetaminophen Tablets, 325 mg, 100-count bottles, Distributed by: Amazon.com Services LLC, 410 Terry Avenue N., Seattle, WA 98109, NDC 72288-405-10

by Aurobindo Pharma USA Inc

Reason
cGMP deviations: Due to confirmed consumer complaints received with the observation of tablet discoloration (brown surface on tablets).
Published
June 25, 2025
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: June 24, 2025Historical recordClass I

RGB Soda, LLC.

Product
Refrigerated Cucumber X Tarragon Ginger Beer (ginger juice).…
Reason
Potential contamination with Salmonella.
Published
June 25, 2025
Distribution
Distributed in WA.

View recall →

FDA Recall United States TerminatedTerminated: September 16, 2026Historical recordClass I

GBC Food Services, LLC

Product
Cucumber Carrot Ranch Pack 20oz 850065403557 Purchase Dates:…
Reason
Potential to be contaminated with Salmonella
Published
June 25, 2025
Distribution
IN, IL, OH, KY, TN, MS, MO, AR and, MI.

View recall →

FDA Recall United States TerminatedTerminated: September 16, 2026Historical recordClass I

GBC Food Services, LLC

Product
Fruit and Veg Tray 64oz 850065403748 Purchase Dates: 05/08/2…
Reason
Potential to be contaminated with Salmonella
Published
June 25, 2025
Distribution
IN, IL, OH, KY, TN, MS, MO, AR and, MI.

View recall →

FDA Recall United States TerminatedTerminated: September 16, 2026Historical recordClass I

GBC Food Services, LLC

Product
Chef Salad 11oz 850065403328 Purchase Dates: 05/08/2025 to 0…
Reason
Potential to be contaminated with Salmonella
Published
June 25, 2025
Distribution
IN, IL, OH, KY, TN, MS, MO, AR and, MI.

View recall →

FDA Recall United States TerminatedTerminated: September 16, 2026Historical recordClass I

GBC Food Services, LLC

Product
Vegetable Bowl $5 13oz 850065403380 Purchase Dates: 05/08/20…
Reason
Potential to be contaminated with Salmonella
Published
June 25, 2025
Distribution
IN, IL, OH, KY, TN, MS, MO, AR and, MI.

View recall →

FDA Recall United States TerminatedTerminated: September 16, 2026Historical recordClass I

GBC Food Services, LLC

Product
Cucumber Bowl with Ranch dip 15oz UPC 850054894519 Purcha…
Reason
Potential to be contaminated with Salmonella
Published
June 25, 2025
Distribution
IN, IL, OH, KY, TN, MS, MO, AR and, MI.

View recall →

FDA Recall United States TerminatedTerminated: July 9, 2025Historical recordClass II

La Fontanella Food Products LLC

Product
Pizza Shoppe The "Pink Stuff" World-Famous Creamy Garlic Sal…
Reason
Potential for product spoilage (increased level of lactic acid detected in retain samples).
Published
June 25, 2025
Distribution
Distribution centers located in MO, KS a…

View recall →

FDA Recall United States TerminatedTerminated: September 5, 2025Historical recordClass II

Yerba Prima Inc

Product
Great Plains Bentonite + Herbal Detox Capsules 60 capsules,…
Reason
Potential contamination with Pseudomonas aeruginosa.
Published
June 25, 2025
Distribution
Distributed in AZ, CA, CO, CT, FL, GA, I…

View recall →

FDA Recall United States TerminatedTerminated: March 19, 2026Historical recordClass I

Reser's Fine Foods, Inc. dba Fresh Creative Foods

Product
Lancaster LF Authentic Greek Salad Kit, 2/7.125lb. packages,…
Reason
Salmonella. Greek Salad Kit made with recalled cucumbers sourced from Bedner Grower's Company which may be contaminated with Salmonella and implicated in an ongoing outbreak.
Published
June 25, 2025
Distribution
Distributed in MA and PA.

View recall →

FDA Recall OngoingHistorical recordClass I

Sulfamethoxazole and Trimethoprim Tablets, USP, 400 mg/80 mg, Rx Only, a) 100 Tablets per Bottle, NDC: 65162-271-10, b) 500 Tablets per Bottle, NDC: 65162-271-50, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral Solid Dosage Unit, Ahmedabad, 382213, INDIA, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807.

by Amneal Pharmaceuticals, LLC

Reason
Microbial contamination of non-sterile products: tablets may exhibit black spots due to microbial contamination.
Published
June 18, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass III

Levothyroxine Sodium Tablets, USP 112 mcg (0.112mg), 1000 tablets, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540. Manufactured by: Macleods Pharmaceuticals Ltd. Sarigam, Valsad, Gujarat, India, NDC 33342-398-44.

by Macleods Pharmaceuticals Ltd

Reason
Presence of a foreign substance: black hair found embedded in tablet.
Published
June 18, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Cephalexin for Oral Suspension, USP, 125 mg per 5 mL, 200 mL (when mixed), Rx Only, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascent Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-544-68

by Ascend Laboratories, LLC

Reason
Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was identified to be Cephalexin Glucose Adduct.
Published
June 18, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Cephalexin for Oral Suspension, USP, 125 mg per 5 mL, 100 mL (when mixed), Rx Only, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascent Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-544-88

by Ascend Laboratories, LLC

Reason
Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was identified to be Cephalexin Glucose Adduct.
Published
June 18, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

Male Ultra Pro, Unleash Your Force 2, 10 capsules per box, Distributed by: Health Fixer Tempe AZ 85288, UPC B0CZN7C6YH.

by SAINI TRADE INC

Reason
Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
Published
June 18, 2025
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.

Reconnecting to the server…

We lost the connection to the server.

Your session has expired.