Class II
Medical Device Recall: Link Patella Glide Resection Guide- For the implantation of the Endo-Model Knee System as part of a total knee arthroplasty procedure. Product Code: 15-2530/05
Waldemar Link GmbH & Co. KG (Mfg Site) · November 30, 2023
Reason for Recall
Mislabeled: Angle and height of the device marked as L(large) corresponds to the small/medium dimensions due to a product mix-up. This may result in too little bone material resected and not fit correctly leading to extended surgery time
Distribution
US Nationwide distribution in the state of NH.
States Affected
NATIONWIDE
Quantity Affected
1 unit
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0749-2024
Status: ongoing
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