FDA Device Intelligence
HomeAvanos Medical, Inc. › ENFit PU Feeding Tube

ENFit PU Feeding Tube

Avanos Medical, Inc. · Model FTXL8.0P-NC · UDI-DI 00350770000695

BSS Prescription
1
510(k) clearances
198
Adverse events (10 deaths)
5
Recalls
11
Facilities

Description

ENFit PU Feeding Tube Orange 8Fr 105cm

Recalls

DateFirmReason
2023-12-20C.R. Bard IncBD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occ
2023-12-20C.R. Bard IncBD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occ
2023-12-20C.R. Bard IncBD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occ
2023-12-20C.R. Bard IncBD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occ
2023-12-20C.R. Bard IncBD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occ

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.