Class II
Medical Device Recall: Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged. Passive safety IV catheter.
B Braun Medical Inc · February 17, 2025
Reason for Recall
Increased risk for valve housing detachment causing leakage.
Distribution
Domestic: CA, CA, FL, GA, IL, IL, IN, MD, MN, MO, NC, NM, NY, PA, TN, TX, VA, and WA; Foreign: Canada.
States Affected
CA, FL, GA, IL, IN, MD, MN, MO, NC, NM, NY, PA, TN, TX, VA, WA
Quantity Affected
28,200 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1397-2025
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.