FDA Enforcement Class II Terminated

UniCel DxC 880i, 860i, 680i, and 660i Integrated Systems, Part Numbers: A64871, A64903, A64935, A59102. The UniCel DxI Immunoassay System is an in vitro diagnostic device used for the quantitative, semi-quantitative or qualitative determination of various analyte concentrations found in human body fluids. The UniCel DxC series of instruments is a DxI Immunoassay System integrated with a chemistry analyzer.

Recall: Z-0347-2013 · Reported November 28, 2012

Enforcement

Recall Number
Z-0347-2013
Event ID
63505
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Beckman Coulter Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Visit
Report Date
November 28, 2012
Initiation Date
August 1, 2011
Classification Date
November 19, 2012
Termination Date
November 19, 2012
Address
250 S Kraemer Blvd, N/A, Brea, CA, 92821-6232, United States

Description

UniCel DxC 880i, 860i, 680i, and 660i Integrated Systems, Part Numbers: A64871, A64903, A64935, A59102. The UniCel DxI Immunoassay System is an in vitro diagnostic device used for the quantitative, semi-quantitative or qualitative determination of various analyte concentrations found in human body fluids. The UniCel DxC series of instruments is a DxI Immunoassay System integrated with a chemistry analyzer.

Reason

The recall was initiated because Beckman Coulter has confirmed that the UniCel Dxl and DxC Access Immunoassay Systems had field modifications to the aspirate and dispense probe assemblies.

Code Info

Serial Numbers: Included in the corresponding Dxl system.

Distribution

Worldwide Distribution - USA (nationwide) and Internationally to Canada, AE, AU, BG, BW, CH, CN, CZ, DE, ES, FR, GB, HK, HR, HU, IN, IT, JO, JP, LB, MA, MX, NL, PL, QA, RO, RU, SK, TN, TR, ZA, AO, AR, AT, BE, CO, DZ, FI, IE, IL, KR, KW, LI, NA, NO, NZ, PF, PH, PR, SE, SG, SZ, TH, TW, VE, VN, and YT.

Quantity

N/A