FDA Enforcement Class II Terminated

UniCel DxH 600 Coulter Cellular Analysis System, Catalog No. B23858.

Recall: Z-2158-2017 · Reported May 31, 2017

Enforcement

Recall Number
Z-2158-2017
Event ID
77145
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Beckman Coulter Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
May 31, 2017
Initiation Date
April 24, 2017
Classification Date
May 24, 2017
Termination Date
May 22, 2018
Address
250 S Kraemer Blvd, Brea, CA, 92821-6232, United States

Description

UniCel DxH 600 Coulter Cellular Analysis System, Catalog No. B23858.

Reason

There is a possibility of a data acquisition disruption that may cause an unusual light scatter event pattern for the white blood cell differential that may not have a system flag and/or message. The events associated with the unusual light scatter pattern may be incorrectly removed from analysis which can result in an erroneous differential result.

Code Info

all software versions

Distribution

Worldwide distribution: US nationwide, Algeria, Andorra, Austria, Australia, Belarus, Belgium, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Canada, China, Colombia, Costa Rica, Cote d'lvoire, Croatia, Czech Republic, Ecuador, France, Germany, Gibraltar, Greece, Hong Kong, Hungary, India, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan , Kuwait, Lebanon, Lithuania ,Macao, Malaysia, Mayotte, Mexico, Morocco, Myanmar, Netherlands, New Zealand, Oman, Pakistan, Panama, Paraguay, Philippines, Poland, Portugal, Puerto Rico, Qatar, Romania , Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia , South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Turkey, United Arab Republic, United Kingdom, Uruguay and Vietnam.

Quantity

1408 units total (998 units in US)