Recall of Device Recall Vaxcel Port with PASV Valve

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Boston Scientific Corporation.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    31251
  • Event Risk Class
    Class 2
  • Event Number
    Z-0780-05
  • Event Initiated Date
    2005-02-25
  • Event Date Posted
    2005-04-28
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2006-08-09
  • Event Source
    USFDA
  • Event Source URL
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Port & Catheter, Implanted, Subcutaneous, Intraperitoneal - Product Code LLD
  • Reason
    Potential separation of the port base from the port cover after implantation.
  • Action
    Letters 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.

Device

  • Model / Serial
    Cat. No. 45-233, including all lots as follows: 910022, 910022D, 923899, 973167, 974706
  • Product Classification
  • Device Class
    Unclassified
  • Implanted device?
    Yes
  • Distribution
    1215 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
  • Product Description
    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.
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Boston Scientific Corporation, 1 Boston Scientific Pl, Natick MA 01760-1536
  • Source
    USFDA