Events

Recall of Becton Dickinson

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

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
    37871
  • Event Risk Class
    Class 2
  • Event Number
    Z-0813-2007
  • Event Initiated Date
    2007-04-09
  • Event Date Posted
    2007-05-24
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2007-08-09
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=52011
  • 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
    syringe - Product Code FMF
  • Reason
    Small cracks in plastic trays of one lot of bd 5ml syringe luer lok tip, bulk sterile convenience paks that may adversely affect tray integrity and steriity.
  • Action
    Recall communications were sent on April 2, 2007 and May 3, 2007 by UPS second day air to all direct consignees and potential customers.

Device

Becton Dickinson

Manufacturer

Becton Dickinson & Company
  • Manufacturer Address
    Becton Dickinson & Company, 1 Becton Dr, Franklin Lakes NJ 07417-1815
  • Manufacturer Parent Company (2017)
    Becton, Dickinson and Company
  • Source
    USFDA