Recall of BD Ophthalmic

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Becton Dickinson and 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
    49436
  • Event Risk Class
    Class 2
  • Event Number
    Z-0022-2009
  • Event Initiated Date
    2008-09-15
  • Event Date Posted
    2008-10-03
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2012-02-29
  • 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
    Ophthalmic Cannula - Product Code HMX
  • Reason
    Product labeled as 4 mm high viscosity injector tip contains a 6 mm tip.
  • Action
    BD contacted accounts by telephone on 9/15/08 requesting users to discard units and complete the response form. Contact Becton Dickinson and Co. at 1-781-906-7950 for assistance.

Device

  • Model / Serial
    Lot Number: 8018591
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    AZ, CA, CO, IL, OH, FL, PA , TN, TX,and VA Foreign: Australia and Japan.
  • Product Description
    BD Visitec High Viscosity Injector, 4mm || Ref: 585173. The product is intended for Vitroretinal Surgery.
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Becton Dickinson and Company, 411 Waverley Oaks Rd Ste 2229, Waltham MA 02452-8448
  • Source
    USFDA