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Recall Observatory FDA recall evidence

Device product

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

Z-0214-2024

October 13, 2023

Class II

Product summary

Firm
Corin Ltd
Event
Event 93144
Status
Ongoing
Classification
Class II
Quantity
1 units
Official record key
device-enforcement:Z-0214-2024

Official wording

Reason: 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.

Code information: UDI/DI 05055343872505, Lot Number 532405.

Distribution pattern: US: MI, TX, IL

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.