Class II
Medical Device Recall: Protege GPS Self-Expanding Peripheral Stent System, product number SERB65-09-60-80, Sterile.
Medtronic Inc. · November 20, 2023
Reason for Recall
Seal defects could compromise the ability of the product packaging to maintain sterility.
Distribution
US Nationwide distribution in the state of MN.
States Affected
NATIONWIDE
Quantity Affected
1
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0623-2024
Status: completed
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.