Home › PHOENIX DIAGNOSTICS, INC. › Phoenix Diagnostics
Phoenix Diagnostics
PHOENIX DIAGNOSTICS, INC. · Model 1009AM · UDI-DI 10852676007145
1
510(k) clearances
3
Adverse events
1
Recalls
18
Facilities
Description
LiquiTrol BGM - Blood Gas / Electrolyte / Metabolite Control - Trilevel
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-09-07 | Radiometer America Inc | Radiometer has recently become aware that a few of the AUTOCHECK 5+ level 2 ampoules, will give incorrect results for pCO2 and pO2. A defective QC ampoule will for: " pCO2 give a r |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.