FDA Device Intelligence
HomeBIO-RAD LABORATORIES, INC. › Liquichek

Liquichek

BIO-RAD LABORATORIES, INC. · Model 572 · UDI-DI 00847661003595

JJS
1
510(k) clearances
3
Adverse events
1
Recalls
18
Facilities

Description

Liquichek Blood Gas Control Level 2 (An aqueous assayed blood gas control.)

Recalls

DateFirmReason
2017-09-07Radiometer America IncRadiometer 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 docs
Data 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.