Recall of Depuy Mitek Fastin

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Depuy Mitek, a Johnson & Johnson Co..

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
    33990
  • Event Risk Class
    Class 2
  • Event Number
    Z-0446-06
  • Event Initiated Date
    2005-10-27
  • Event Date Posted
    2006-01-26
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2006-05-02
  • 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
    Fastener, Fixation, Biodegradable, Soft Tissue - Product Code MAI
  • Reason
    The device may contain one strand of suture instead of two strands.
  • Action
    DePuy Mitek initiated the recall to domestic accounts by letter on 10/27/05 and to J & J Affiliates by email.

Device

  • Model / Serial
    Lot Number:1270449
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    CA, IA, FL, MI, MO, OR, TX Foreign:Australia, Brazil, Sweden
  • Product Description
    Depuy Mitek Fastin RC Anchor with Panacryl (2) strands Size 2 Panacryl Poly ***braided absorbable suture || Reference Number: 222740
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Depuy Mitek, a Johnson & Johnson Co., 325 Paramount Dr, Raynham MA 02767-5199
  • Source
    USFDA