Recall of Device Recall UniCel DxH Slidemaker Stainer

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Beckman Coulter 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
    78611
  • Event Risk Class
    Class 2
  • Event Number
    Z-0238-2018
  • Event Initiated Date
    2017-11-03
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2018-06-19
  • 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
    Counter, differential cell - Product Code GKZ
  • Reason
    The shield for the single-tube station on the dxh instrument may interfere with sample aspiration in the open vial position.
  • Action
    The firm notified its consignees of the recall on 11/03/2017 by letter. The letter stated the issue and provided the following instructions: ¿ "To avoid a biohazardous spill, do not use the right (green) position of the Single-Tube Station for sample aspiration until the shield is removed. ¿ You may remove the shield following the instructions in Attachment 1 or contact your local Beckman Coulter Representative for further assistance."

Device

  • Model / Serial
    Serial Numbers: AW09034, AV40142, AU19113
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    CA, AR, HI, CA, OH, WA, MD, Canada, Japan
  • Product Description
    UniCel DxH Slidemaker Stainer, Part Number 75222, for use with automated hematology analyzer
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Beckman Coulter Inc., 250 S Kraemer Blvd, Brea CA 92821-6232
  • Manufacturer Parent Company (2017)
  • Source
    USFDA