OtherGKR
RAPIDPOINT 500
Received Jan 15, 2013 · Event occurred Dec 13, 2012
Report 1217157-2012-00081 · MDR key 2929377
Device
Generic name
Rapidpoint 500
Model number
500Product problems
- Incorrect, Inadequate or Imprecise Result or Readings
Patient
Not reported
- No Consequences Or Impact To Patient
Narrative
Additional Manufacturer Narrative
CUSTOMER CLAIMS THE DISCORDANT RESULTS ARE BEYOND THE BIOLOGICAL ALLOW ERROR OF 5.4% FOR PCO2.
Description of Event or Problem
CUSTOMER REPORTS DISCREPANT PCO2 RESULTS. THERE IS NO REPORT OF INJURY WITH THIS EVENT.