Introcan Safety 3 IV Catheter (B Braun) – Valve Housing Risk (2025)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged. Passive safety IV catheter.
Brand
B Braun Medical Inc
Lot Codes / Batch Numbers
Model No 4251128-02, UDI-DI 04046964014017, Lot 24F09G8952.
Products Sold
Model No 4251128-02; UDI-DI 04046964014017; Lot 24F09G8952.
B Braun Medical Inc is recalling Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged. Passive safety IV catheter. due to Increased risk for valve housing detachment causing leakage.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Increased risk for valve housing detachment causing leakage.
Recommended Action
Per FDA guidance
An URGENT MEDICAL DEVICE RECALL NOTIFICATION dated 2/13/25 was mailed to consignees notifying them of this product removal. Consignees are instructed to review the recall notification and to forward the notice along to those in their organization and to those to which product was further distributed. Consignees are to quarantine any affected devices in their inventory and coordinate product return by completion and return of the provided Product Recall Acknowledgement Form. Consignees with any questions are to contact B Braun at 844-903-6417.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, FL, GA, IL, IN, MD, MN, MO, NM, NY, NC, PA, TN, TX, VA, WA
Page updated: Jan 10, 2026