ClearanceBrief
Recall Z-1464-06 · CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph

Siemens Healthcare Diagnostics

RapidLab 1200 Systems, Model 1245 - Blood gases, electrolyte and blood pH test system, Bayer HealthCare LLC, Diagnostics Division

DateAug 29, 2006 (initiated Apr 4, 2006)
StatusTerminated
ReasonInvalid CO-oximeter values; Bayer HealthCare determined that under very specific conditions, the RapidLab 1245 or RapidLab 1265 systems may report invalid CO-oximeter values to an LIS, Rapidlink, or Rapidcomm™ data management system.
Root causeSoftware design
ActionOn 4/04/06, Bayer HealthCare LLC (Diagnostics Division) sent Support Bulletins to all affected Bayer HealthCare LLC Branches via e-mail in order to inform them of the issue, and to provide them with instructions for the interim work-around until the new software version is installed. Customer Bulletins were prepared and sent to the Branches both in the United States and globally for communication with the affected customers.
QuantityDomestic - 124 units, Foreign-364 units (all systems)
DistributionWorldwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K031560BAYER RAPIDLAB 1200 SYSTEM
Bayer Healthcare, LLC, Dec 17, 2003