Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur Recalled by Stanmore Implants Worldwide Ltd. Due to Three (3) complaints were identified in which the...
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
JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur is intended for the replacement of diseased or deficient bone in the distal femur.
Quantity: 15 units
Why Was This Recalled?
Three (3) complaints were identified in which the potential for utilization of the JTS Grower Drive in the incorrect orientation in relation to the limb entry point of the device, together with the potential to select incorrect settings for the extension procedure. As a result, the prostheses in such cases failed to extend as intended.
Where Was This Sold?
This product was distributed to 10 states: CA, FL, GA, KS, MI, NJ, OH, PA, SC, TX
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