M/dn Intramedullary Fixation Humeral Guide Wire - Smooth, Zms Intramedullary Fixation Smooth Guide Wire, Zimmer Natural Nail System - Tear Drop Guide Wire, And Pressure Sentinel Intramedullary Reami
Recall Summary Four intramedullary guide wire products used in orthopedic surgery are being recalled across Canada due to issues with the medical devices themselves. The recalled products are the M/DN Intramedullary Fixation Humeral Guide Wire, ZMS Intramedullary Fixation Smooth Guide Wire, Zimmer Natural Nail System Tear Drop Guide Wire, and Pressure Sentinel Intramedullary Reamer. This is a Class I recall, meaning the most serious classification, affecting patients who may have received these devices during bone repair procedures.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-11-28
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/31075977-ff5c-4d3b-81cf-463651416c97