In the agency's Nov 11, 2026 enforcement report · Ongoing

Unity Knee ASC Modular Handle included in the Corin UNITY ASC INSTRUMENT SYSTEM. Part Number: 1232040.

Corin Medical, Ltd.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: CORIN MEDICAL, LTD. · Unit 1-57-8, Corinium Centre · Cirencester

Is this the product you have?

  • Unity Knee ASC Modular Handle included in the Corin UNITY ASC INSTRUMENT SYSTEM
  • Part Number1232040
Lot codes and dates
  • Part Number
    • 1232040. UDI-DI/GTIN
    • 05056139239656
  • Lot Code097921
Amount recalled
22 units

Where it was sold

Why it was recalled

Potential malfunction of the Modular Handles where the locking mechanism may fail. Any mating instruments already engaged to the handle will not be able to be disengaged, and the handle will be unable to fitted securely to any unengaged mating instruments.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Nov 4, 1:42 PM UTC

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