Recall of Weck Hemoclip Plus Ligating Clips

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

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
    29820
  • Event Risk Class
    Class 2
  • Event Number
    Z-1391-04
  • Event Initiated Date
    2003-10-24
  • Event Date Posted
    2004-08-24
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2004-08-25
  • 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
    Applier, Hemostatic Clip - Product Code HBT
  • Reason
    Hole in the sterile unit blister pack that could compromise sterility.
  • Action
    The consignees were notified of the recall via letter beginning October 24, 2003 asking for return of the product.

Device

  • Model / Serial
    All lots manufactured between 2001-8 thorugh 2002-12 for all three products and lot 763100 for 25 Medium Titanium Clips, lots 763102 and 949861 for 25 Small Clips and lot 814007 for 10 Large Titanium Clips
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide and to accounts in Canada, Europe Asia, and South/Latin America
  • Product Description
    Ref. No. 533702 Hemoclip Plus, 25 Medium Titanium Clips, No Tape; Ref. No. 533737 Hemoclip Plus, 25 Small Titanium Clips/Cartridge, No Tape and Ref. No. 533872 Hemoclip Plus, 10 Large Titanium Clips/Cartridge, No Tape
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Weck, 1 Weck Dr., Research Triangle Park NC 27709
  • Source
    USFDA