ClearanceBrief
Recall Z-0780-05 ยท LLD Port & Catheter, Implanted, Subcutaneous, Intraperitoneal

Boston Scientific Corporation

Vaxcel Low Profile Port with PASV Valve and 6F Polyurethane Catheter. CATALOG NO. 45-233. Ref. # M001452330. FIRM ON LABEL: Boston Scientific MEDI-TECH. Manufactured for: Boston Scientific Corp., One Boston Scientific Place, Natick, MA 01760-1537. Manufactured at: 10 Glens Falls Technical Park, Glens Falls, NY 12801.

DateApr 28, 2005 (initiated Feb 25, 2005)
StatusTerminated
ReasonPotential separation of the port base from the port cover after implantation.
Root causeOther
ActionLetters sent 3/11/2005 via Federal Express to hospitals receiving affected product. Customers instructed to remove/return product, notify physicians, evaluate patients and explant devices whenever possible.
Quantity160 units
Distribution1215 units shipped to 123 hospitals throughout the U.S. 2 units shipped to Boston Scientific in South Africa where 1 unit had been used as a demo (non-human use) and 1 units is in BSC control
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K032600VAXCEL PORT, MODEL 45-333 AND VAXCEL W/PASV PORT, MODEL 45-233
Boston Scientific Corp, Sep 9, 2003