Events

Recall of Synchron LXi 725

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
    58567
  • Event Risk Class
    Class 1
  • Event Number
    Z-2132-2011
  • Event Initiated Date
    2011-04-05
  • Event Date Posted
    2011-05-06
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2013-02-06
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=99602
  • 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
    Discrete Photometric Chemistry Analyzer for Clinical Use - Product Code JJE
  • Reason
    The recall was initiated because beckman coulter has received reports of incorrect electrolyte results on synchron lx systems due to a variety of maintenance-related hardware issues.
  • Action
    The recall communication was initiated on 04/05/2011 with Beckman Coulter forwarding a Product Correction letter with attached customer response form to the affected customers via US Postal Service. The letter informed customers of the products affected, the issue, the impact, and the actions to be taken. Customers were instructed to follow the steps provided in order to address the issues related to microbial contamination; and to complete and return the enclosed response form within 10 days so that receipt of this important information could be confirmed. In addition, the letter requested customers share the information with their laboratory staff and retain the notification as part of your laboratory Quality System documentation. For customers who have any questions regarding this update, the letter indicated to contact Customer Support Center Call Center via the Beckman Coulter website at http://www.beckmancoulter.com/customersupport/support/. They may also contact Beckman Coulter at (800) 854-3633 in the United States and Canada or through your local Beckman Coulter representative. Beckman Coulter will issue two additional recall notification ("UPDATE TO URGENT PRODUCT CORRECTION Synchron LX20, LX20 PRO, LXi 725 Clinical Systems") beginning on 05/20/2011, one to Laboratory Directors and one to Physicians. The notices will be mailed via US Postal Service on Friday, May 20th. Customers who have subscribed to email notifications will receive an email containing the letters on Monday, May 23th. Both letter informs the Laboratory Directors and Physicians that Beckman Coulter has received reports of erroneous/aberrant sodium, potassium, chloride and calcium results that have been released from the laboratory. Electrolyte shifts can be low or high and may occur above, below or within the normal range. Laboratory Directors were instructed to immediately disseminate the Attachment to this letter (via notification/alert procedure appropriate to your

Device

Synchron LXi 725
  • Model / Serial
    All Serial Numbers.
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution -- Australia, Belgium, Canada, China, Colombia, Czech Republic, Ecuador, Egypt, Finland, France, French Polynesia, Germany, Hong Kong, India, Ireland, Italy, Japan, Republic of Korea, Kuwait, Mexico, Netherlands, Oman, Panama, Philippines, Puerto Rico, Saudi Arabia, Singapore, Slovakia, South Africa, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, and the United States.
  • Product Description
    Synchron LXi 725, Part Number: 476501. || Designed for the in vitro determination of a variety of general chemistries, therapeutic drugs, and other chemistries.
  • Manufacturer
    Beckman Coulter Inc.

Manufacturer

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