Home › Device types › ECX
Cylinder, Compressed Gas, And Valve
FDA product code ECX · Class 1 · Anesthesiology
33
Registered devices
96
Adverse events
15
Recalls
13
510(k) clearances
Devices with this code
Resp-O2 M6 Oxygen B-Cylinder,1L With CGA870 Post Valve — Dynarex CorporationLIFE®Cylinder — Mv Life LLCCeodeux S.A - Meditec — CEODEUX S.A.Resp-O2 M15 Oxygen Jumbo D-Cylinder 2.9 L with CGA870 Toggle Valve — Dynarex CorporationCeodeux S.A - Meditec — CEODEUX S.A.Resp-O2 M15 Oxygen Standard D-Cylinder 2.89 L, With CGA 870 Post Valve — Dynarex CorporationICON 2 — Control Devices, LLCLIFE®Cylinder — Mv Life LLCCeodeux S.A - Meditec — CEODEUX S.A.Control Devices — Control Devices, LLCLIFE®Cylinder — Mv Life LLCLIFE®Cylinder — Mv Life LLCResp-O2 M24 Oxygen E-Cylinder 4.6 L with CGA870 Toggle Valve — Dynarex CorporationCeodeux S.A - Meditec — CEODEUX S.A.Ceodeux S.A - Meditec — CEODEUX S.A.Ceodeux S.A - Meditec — CEODEUX S.A.iFill — Control Devices, LLCCeodeux S.A - Meditec — CEODEUX S.A.ICON 2 / Virtair — Control Devices, LLCCeodeux S.A - Meditec — CEODEUX S.A.LIFE®Cylinder — Mv Life LLCiFill — Control Devices, LLCCeodeux S.A - Meditec — CEODEUX S.A.Ceodeux S.A - Meditec — CEODEUX S.A.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-10-16 | Western/Scott Fetzer Company | VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the plastic VIPR shroud to break apart with emission of fumes and smoke |
| 2019-08-15 | Western / Scott Fetzer Company | Limited access to flow settings as a result of the control knob having been rotated beyond its functional range |
| 2019-08-15 | Western / Scott Fetzer Company | Limited access to flow settings as a result of the control knob having been rotated beyond its functional range |
| 2019-08-15 | Western / Scott Fetzer Company | Limited access to flow settings as a result of the control knob having been rotated beyond its functional range |
| 2019-08-15 | Western / Scott Fetzer Company | Limited access to flow settings as a result of the control knob having been rotated beyond its functional range |
| 2019-08-15 | Western / Scott Fetzer Company | Limited access to flow settings as a result of the control knob having been rotated beyond its functional range |
| 2009-05-15 | Allied Healthcare Products Inc | Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open p |
| 2009-05-15 | Allied Healthcare Products Inc | Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open p |
| 2009-05-15 | Allied Healthcare Products Inc | Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open p |
| 2009-05-15 | Allied Healthcare Products Inc | Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open p |
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 docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
