Boston Scientific Corporation Vaxcel Port with PASV Valve, 8 Fr polyurethane catheter, Mini Titanium port, Implantable Port System, Model # M001452150, Catalog #45-215 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Vaxcel Port with PASV Valve, 8 Fr polyurethane catheter, Mini Titanium port, Implantable Port System, Model # M001452150, Catalog #45-215
Brand
Boston Scientific Corporation
Lot Codes / Batch Numbers
866561, 876068, 885270, 885444, 886041, 886398, 887738, 888993, 889702, 890163, 903721
Products Sold
866561, 876068, 885270, 885444, 886041, 886398, 887738, 888993, 889702, 890163, 903721
Boston Scientific Corporation is recalling Vaxcel Port with PASV Valve, 8 Fr polyurethane catheter, Mini Titanium port, Implantable Port System due to Reports of catheter separation/fracture after implantation resulting in distal migration of the catheter.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Reports of catheter separation/fracture after implantation resulting in distal migration of the catheter.
Recommended Action
Per FDA guidance
Letters dated 2/9/04 with instructions to return current inventory . Also included is information concerning implanted ports.
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 noticePage updated: Jan 10, 2026