Recall Z-0353-2019

Beckman Coulter Inc. · initiated May 24, 2018

Class III Terminated

Class III – products unlikely to cause any adverse health reaction but that violate FDA labeling or manufacturing laws

Product

Intelligent Peri-Analytical Workstation (HW+SW), Catalog #: A89492 (iPAW Software v4.2.1), Beckman Coulter, Inc. The iPAW ((intelligent Peri-Analytical Workstation) can act as: a software client for specimen tracking and workload statistics or a physical workstation for manual sorting and label printing.

Codes / lots: v4.2.1 (and 4.2, discontinued)

Reason for recall

Sorting-Drive software version 4.2 (released in October 2015) introduced a new option for iPAW and the Sorting-Drive Client that is used for manual printing of barcodes. Sorting Drive software version 4.2 was replaced by 4.2.1 (both versions contain the same option for manual barcode printing). When printing consecutively numbered tube labels using this optional Barcode Counter function, the system incorrectly converts numbers with consecutive multiple zeroes in the middle, potentially leading to wrong barcode IDs. The firm reports this does not affect automated label creation or reprinting of individual labels and that no other system functions are affected.

FDA-determined cause: Software change control

Action taken

On 6/4/2018 Beckman Coulter (BEC) reported that the issue will be corrected via a field modification performed by Field Service. BEC reported that they do not intend to send a customer letter for this issue.US customers can contact the Technical Support Troubleshooting Hotline at (800) 854-3633.

Details

Recall number
Z-0353-2019
Initiated
May 24, 2018
Terminated
December 8, 2022
Product code
JQP – Calculator/Data Processing Module, For Clinical Use
Quantity
283
Distribution
Worldwide Distribution: US (nationwide) and countries of: Algeria, Argentina, Austria, Belgium, Brazil, Chile, China, Czech Republic, Denmark ,France, Germany, Greece ,Hong Kong, India, Ireland, Israel, Italy ,Republic of Korea, Lebanon, Lithuania ,Malaysia, Netherlands, Poland, Portugal , Qatar, Romania, Russian Federation, Saudi Arabia ,South Africa , Spain, Sweden, Taiwan, Turkey , and United…
Recalling firm
Beckman Coulter Inc., Brea, CA

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0354-2019 Class IIISoftware Package, Sorting-Drive 4.2 User Kit, Part No. B73488, Manufactured by: Beckman…Sorting-Drive software version 4.2 (released in October 2015) introduced a new option which included the… 05/24/2018Terminated
Z-0355-2019 Class IIISoftware Package, Sorting-Drive 4.2.1 User Kit for Windows XP and Windows 10, Part No.…Sorting-Drive software version 4.2 (released in October 2015) introduced a new option which included the… 05/24/2018Terminated
Z-0356-2019 Class IIISoftware Package, iPAW 4.2 User Kit, Part No. B73489, Manufactured by: Beckman Coulter…Sorting-Drive software version 4.2 (released in October 2015) introduced a new option for iPAW and the… 05/24/2018Terminated
Z-0357-2019 Class IIISoftware Package, iPAW 4.2.1 User Kit for Windows XP and Windows 10, Part No. B95343…Sorting-Drive software version 4.2 (released in October 2015) introduced a new option for iPAW and the… 05/24/2018Terminated
Z-0358-2019 Class IIISorting-Drive Product Part, Sorting-Drive Plus Kit (Sorting Drive Software v4.2.1), Part…Sorting-Drive software version 4.2 (released in October 2015) introduced a new option for iPAW and the… 05/24/2018Terminated
Z-0359-2019 Class IIISorting-Drive Professional Part, Sorting-Drive Professional Kit, (Sorting Drive Software…Sorting-Drive software version 4.2 (released in October 2015) introduced a new option for iPAW and the… 05/24/2018Terminated