Gem Flex Coil And Interface P-connector (2016-02-15)

Recall Summary The GEM Flex Coil and Interface P-Connector medical devices are being recalled across Canada because they do not meet required safety and performance standards. This Class I recall affects devices distributed throughout Canada. These products are used in medical applications and their malfunction could potentially cause patient harm.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-02-22
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f722230a-242f-4860-824b-bb0d8617d45a