Recall of Device Recall Boston Scientific /Micorvasive

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
    26713
  • Event Risk Class
    Class 2
  • Event Number
    Z-1061-03
  • Event Initiated Date
    2003-07-03
  • Event Date Posted
    2003-07-29
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2004-06-17
  • 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
    Instrument, Biopsy - Product Code KNW
  • Reason
    Sterility of the device may be compromised due to a lack of package integrity.
  • Action
    Boston Scientific notified accounts by letter on 7/3/03. Accounts are requested to check inventory and return product. A Veification Form was requested to be completed.

Device

  • Model / Serial
    4104836, 4145036, 4211323, 4290090 ,4370503 4405122, 4445839, 4461241, 4569317, 4666229 4916051, 5022356, 5120746, 5133248, 5251508,  5288530
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    ASAP Channel Cut Biopsy System, 14 gauge || Reference Number: 1250
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Boston Scientific Corporation, 1 Boston Scientific Place, Natick MA 01760
  • Source
    USFDA