Home › Device types › FEG
Tube, Double Lumen For Intestinal Decompression And/Or Intubation
FDA product code FEG · Class 2 · Gastroenterology, Urology
134
Registered devices
342
Adverse events
14
Recalls
13
510(k) clearances
Devices with this code
Salem Sump — Cardinal Health, Inc.Axiom® Uni-Sump — AXIOM MEDICAL, INCORPORATEDSalem Sump — Cardinal Health 200, LLCSalem Sump — Cardinal Health 200, LLCSalem Sump — Cardinal Health 200, LLCSalem Sump — Cardinal Health, Inc.Bard® Nasogastric Sump Tube with PreVent® Anti-Reflux Filter — C. R. Bard, Inc.Axiom® Mills Sump — AXIOM MEDICAL, INCORPORATEDSalem Sump — Cardinal Health, Inc.Axiom® Uni-Sump — AXIOM MEDICAL, INCORPORATEDAxiom® Mills Sump — AXIOM MEDICAL, INCORPORATEDSalem Sump — Cardinal Health, Inc.Cook — COOK IRELAND LTDBard® Nasogastric Sump Tube and PreVent® Filter and Lopez Valve® with ENFit™ — C. R. Bard, Inc.Salem Sump — Cardinal Health 200, LLCBard® Nasogastric Sump Tube and PreVent® Filter and Lopez Valve® with ENFit™ — C. R. Bard, Inc.Axiom® Dual-Sump — AXIOM MEDICAL, INCORPORATEDBilbao Dotter — COOK INCORPORATEDAxiom® Hacienda Sump® — AXIOM MEDICAL, INCORPORATEDSalem Sump — Cardinal Health, Inc.Bard® Nasogastric Sump Tube with PreVent® Anti-Reflux Filter with ENFit™ — C. R. Bard, Inc.Bard® Nasogastric Sump Tube with PreVent® Anti-Reflux Filter — C. R. Bard, Inc.Salem Sump — Cardinal Health 200, LLCBard® Nasogastric Sump Tube with PreVent® Anti-Reflux Filter and Lopez Valve® — C. R. Bard, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-09-18 | Cardinal Health 200, LLC | Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expans |
| 2025-09-18 | Cardinal Health 200, LLC | Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expans |
| 2024-07-24 | Cardinal Health 200, LLC | The firm received reports of breakage in the Anti-Reflux Valve (ARV) due to improper use. As a result, changes to labeling were made. |
| 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, decompressi |
| 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, decompressi |
| 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, decompressi |
| 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, decompressi |
| 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, decompressi |
| 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, decompressi |
| 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, decompressi |
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