FDA Device Intelligence
Home › FIM MEDICAL › Pipette

Pipette

FIM MEDICAL · Model Pipette · UDI-DI 03760253450263

CCJ
1
510(k) clearances
0
Adverse events
1
Recalls
12
Facilities

Recalls

DateFirmReason
2025-04-21Capnia IncSampling set nasal cannula used with End-Tidal Carbon Monoxide (ETCO) monitor may have residual carbon monoxide and volatile organic compounds present due to insufficient aeration

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.