FDA Adverse Event
Injury
Summary report: N
CUSTOMIZED FLEX-TEND, CUFFLESS
MDR report key: 147974
·
Received February 6, 1998
Report
- Report Number
- 1824231-1998-00001
- Event Type
- Injury
- Date Received
- February 6, 1998
- Date of Event
- December 15, 1997
- Report Date
- January 14, 1998
- Manufacturer
- BIVONA MEDICAL TECHNOLOGIES
- Product Code
- BTO
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SW
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
SILICONE "GODS" DESTROYED ON THREE LOCATIONS. THE TUBE HAS BEEN IN PT FOR 2 WEEKS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CUSTOMIZED FLEX-TEND, CUFFLESS | TRACHEOSTOMY TUBE | BTO | BIVONA MEDICAL TECHNOLOGIES | C7TTFT604.5006 | CL0820 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 7 YR | Hospitalization |