Class II
Medical Device Recall: Medtronic Disposable Pressure Display Sets: a) DLP¿ 114.3 cm (45 in), Model Number 61000; b) DLP¿ 114.3 cm (45 in), Model Number 62000
Medtronic Perfusion Systems · March 19, 2024
Reason for Recall
Potential for unsealed sterile packing.
Distribution
Worldwide distribution.
Quantity Affected
1624 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1802-2024
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.