Zimmer Air Dermatome II Handpiece And Width Plates (2016-07-11)

Zimmer Air Dermatome II Recall Summary Zimmer Air Dermatome II handpieces and width plates are being recalled in Canada because they are medical devices that do not meet required safety and performance standards. The recall applies to all units distributed across Canada. This device is used in medical settings for skin grafting procedures.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-07-22
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/acdc2c01-237c-4634-a05e-de40efff25d0