RecallWatchUSA

Home / Recalls / Medical Devices

Corin Ltd recalls Unity Total Knee System, Model Number 112.001.34. Primary and revision total knee arthroplasty

Recalled November 8, 2023 · FDA recall Z-0214-2024 · Corin

Hazard
Potential for Unity CR Inserts Right size 6 from batch 529803 to be incorrectly labelled as Unity CR Inserts Right size 7 from batch 532405 and visa versa. · FDA Class II
Units
1 units
Sold at
US: MI, TX, IL

Description

Potential for Unity CR Inserts Right size 6 from batch 529803 to be incorrectly labelled as Unity CR Inserts Right size 7 from batch 532405 and visa versa.

Product
Unity Total Knee System, Model Number 112.001.34. Primary and revision total knee arthroplasty
Manufacturer(s)
Corin Ltd
Made in
United Kingdom

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Corin Ltd recalls Unity Total Knee System, Model Number 112.001.34. Primary and revision total knee arthroplasty | RecallWatchUSA