Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Distal Femoral Replacement (patient specific Recalled by Stanmore Implants Worldwide Ltd. Due to Incorrect component used to manufacture distal femoral replacement.
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 Stanmore Implants Worldwide Ltd. directly.
Affected Products
Distal Femoral Replacement (patient specific, custom made orthopedic implant device). PIN 19960
Quantity: 1
Why Was This Recalled?
Incorrect component used to manufacture distal femoral replacement.
Where Was This Sold?
This product was distributed to 1 state: OH
About Stanmore Implants Worldwide Ltd.
Stanmore Implants Worldwide Ltd. has 8 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report