Home › NEOMED, INC. › NeoMed Enteral Feeding Tube
NeoMed Enteral Feeding Tube
NEOMED, INC. · Model FTS4.0P-EO · UDI-DI 00817584011069
10
510(k) clearances
198
Adverse events (10 deaths)
5
Recalls
11
Facilities
Description
Polyurethane Enteral Feeding Tube, 4.0 Fr x 40 cm, EO
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-12-20 | C.R. Bard Inc | BD (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 |
| 2023-12-20 | C.R. Bard Inc | BD (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 |
| 2023-12-20 | C.R. Bard Inc | BD (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 |
| 2023-12-20 | C.R. Bard Inc | BD (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 |
| 2023-12-20 | C.R. Bard Inc | BD (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 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.
