Class II
Medical Device Recall: REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly
Stryker Sustainability Solutions · May 31, 2024
Reason for Recall
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.
Distribution
US Nationwide distribution in the states of CA, CO, IL, MI, OR, WI.
States Affected
NATIONWIDE
Quantity Affected
90 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2405-2024
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.