Product Wiki · Recalls · Health Canada — Medical Devices

T2 Ankle Arthrodesis Nail, IEFT, Non-Sterile, T2 Femur System — recall 60906

Health Canada — Medical Devices · Canada · 2018-05-04 · Type I

As described by Health Canada — Medical Devices: T2 Ankle Arthrodesis Nail, IEFT, Non-Sterile, T2 Femur System - Femoral Nails, T2 Tibial Nail System - Nail Standard (Sterile) and T2 Recon Nail System - Titanium (2018-04-24)

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
60906
Date of alert
2018-05-04
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: On April 9, 2018, the manufacturer discovered that potentially out-of-specification products may have left the factory. To date, there have been no customer complaints logged for this issue. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/t2-ankle-arthrodesis-nail-ieft

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