Corin Ltd: Medical Device Recall in 2023 - (Recall #: Z-0213-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Unity CR Femur Right, Size 6, Model Number 112.001.32 Primary and revision total knee arthroplasty

Product Classification:

Class II

Date Initiated: October 13, 2023

Date Posted: November 8, 2023

Recall Number: Z-0213-2024

Event ID: 93144

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 3 units

Code Information:

UDI/DI: (05055343872499, Lot Number: 529803.

Distribution Pattern:

US: MI, TX, IL

Voluntary or Mandated:

Voluntary: Firm initiated