Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to The firm discovered through customer complaints that device...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Waldemar Link GmbH & Co. KG (Mfg Site) directly.
Affected Products
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left
Quantity: 22 units
Why Was This Recalled?
The firm discovered through customer complaints that device segments may not meet specifications.
Where Was This Sold?
This product was distributed to 8 states: AL, GA, IL, IN, KS, NJ, NY, TX
About Waldemar Link GmbH & Co. KG (Mfg Site)
Waldemar Link GmbH & Co. KG (Mfg Site) has 62 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report