Home › Precision Medical, Inc. › 1MFA Flowmeters
1MFA Flowmeters
Precision Medical, Inc. · Model Y1MFAPCFP · UDI-DI 00850027043142
CAX
Prescription
10
510(k) clearances
156
Adverse events (15 deaths)
1
Recalls
45
Facilities
Description
1MFA SERIES,Y,FM,O2,70LPM & 26LPM,POLE CLAMP,FISHER & PAYKEL
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-08-26 | Porter Instrument Co Inc | inverted check value on the bag tee assembly which can cause leaking of mixed N2O/O2 gas |
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.