Dult IV Set With Rate Flow Regulator, Rate Flow Regulator Extension Set, And Rate Flow Regulator IV Set (2018-10-01)

IV Set Recall Summary Abbott is recalling Adult IV Sets with Rate Flow Regulators and related extension sets distributed across Canada because the devices may not deliver medication at the intended rate due to a potential defect in the regulator mechanism. This could result in patients receiving incorrect medication doses. The recall affects all IV sets of this type that were distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-10-26
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2c50e459-0c3a-4a44-b2cf-9e7b6148fc1e