Class II
Medical Device Recall: Medtronic Tourniquet Sets: a) DLP¿ 5.5 in (14.0 cm) Tourniquet Kit, Model Number 79004, b) DLP¿ 7 in (17.8 cm) Tourniquet Kit, Model Number 79009
Medtronic Perfusion Systems · March 19, 2024
Reason for Recall
Potential for unsealed sterile packing.
Distribution
Worldwide distribution.
Quantity Affected
1760 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1798-2024
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.