FDA Adverse Event
Death
Summary report: N
INTELLIOX PLUS
MDR report key: 15089015
·
Received July 22, 2022
Report
- Report Number
- 3003764448-2022-00001
- Event Type
- Death
- Date Received
- July 22, 2022
- Date of Event
- July 17, 2022
- Report Date
- July 17, 2022
- Manufacturer
- CEODEUX S.A.
- Product Code
- CAN
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
Description of Event or Problem · 0
CUSTOMER ALLEGES THAT CYLINDER GAUGE MAY HAVE MALFUNCTIONED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 546954 | INTELLIOX PLUS | GAS CYLINDER REGULATOR | CAN | CEODEUX S.A. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Unknown | Death |