Class II

Medical Device Recall: Medtronic Clearview Blower/Mister, Model Number 22120

Medtronic Perfusion Systems · March 19, 2024

Reason for Recall

Potential for unsealed sterile packing.

Distribution

Worldwide distribution.

Quantity Affected

500 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1794-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.