Recall Z-0002-2013

Beckman Coulter Inc. · initiated January 20, 2012

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

COULTER PrepPlus, Part Number: 286600 Product Usage: The COULTER PrepPlus, is a microprocessor-controlled pipetting and diluting system, designed for automating sample preparation or assay methods. It is capable of aspirating and dispensing liquid samples.

Codes / lots: All Serial Numbers

Reason for recall

The recall was initiated because Beckman Coulter has confirmed that the Coulter PrepPlus may experience intermittant reagent level sense failures where the instrument may not produce a warning that a reagent vial is low or out of reagent.

FDA-determined cause: Device Design

Action taken

Beckman Coulter sent an Urgent Product Correction letter dated January 20, 2012 to all their customers who purchased the affected product. The letter provides the customers with an explanation of the problem identified and actions to be taken. Customers were instructed to complete and return the Response Form with in 10 days. Customers with questions regarding the PCA letter were instructed to contact Beckman Coulter Service at (800) 526-7694 in the US and Canada or contact their local Beckman Coulter Representative.

Details

Recall number
Z-0002-2013
Initiated
January 20, 2012
Posted by FDA
October 1, 2012
Terminated
October 2, 2012
Product code
JQW – Station, Pipetting And Diluting, For Clinical Use
Quantity
36 units total (15 units in the US)
Distribution
Worldwide Distribution - US Nationwide and the countries of: Australia, Botswana, Canada, France, Germany, Japan, Malawi and Sweden.
Recalling firm
Beckman Coulter Inc., Brea, CA

Official FDA recall record