Events

Recall of Device Recall Four Shooter Saeed MultiBand Ligator

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Wilson-Cook Medical Inc.

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
    28200
  • Event Risk Class
    Class 3
  • Event Number
    Z-0536-04
  • Event Initiated Date
    2004-01-15
  • Event Date Posted
    2004-07-20
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2004-09-14
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=31368
  • 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
    Ligator, Hemorrhoidal - Product Code FHN
  • Reason
    Product label lacks the symbols specifying the meaning of the manufacturing and expiration date.
  • Action
    Consignee was notified by letter, hand delivered by Cook sales representative on 1/19/2004.

Device

Device Recall Four Shooter Saeed MultiBand Ligator
  • Model / Serial
    Reorder/Catalog number MBL-4-XL, Lot W1842922
  • Product Classification
    Gastroenterology-Urology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    All units were shipped to one medical facility in CA
  • Product Description
    Four Shooter Saeed Multi-Band Ligator
  • Manufacturer
    Wilson-Cook Medical Inc

Manufacturer

Wilson-Cook Medical Inc
  • Manufacturer Address
    Wilson-Cook Medical Inc, 5951 Grassy Creek Blvd, Winston Salem NC 27105-1206
  • Source
    USFDA