FDA Adverse Event
Injury
Summary report: N
MALLINCKRODT
MDR report key: 2926295
·
Received January 16, 2013
Report
- Report Number
- 2936999-2013-00036
- Event Type
- Injury
- Date Received
- January 16, 2013
- Date of Event
- May 22, 2012
- Report Date
- December 18, 2012
- Manufacturer
- COVIDIEN, FORMERLY TYCOHEA, AVENIDA HENEQUEN
- Product Code
- BTR
- PMA / PMN Number
- K090352
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- NOT APPLICABLE
Narratives
Description of Event or Problem · 1
CUSTOMER STATES: AFTER 2 DAYS USE ON A PATIENT AT HOSPITAL, A DOCTOR CONFIRMED THE PATIENT DEVELOPED PHARYNGEAL EDEMA AND HE HAD TO PERFORM THE TRACHEOSTOMY. THE INTUBATION WAS PERFORMED BY USE OF PHARYNGOSCOPE. CURRENTLY THE PATIENT IS RECOVERED. PRE-TEST WAS DONE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 25105 | MALLINCKRODT | TAPERGUARD ORAL/NASAL TRACHEAL TUB | BTR | COVIDIEN, FORMERLY TYCOHEA, AVENIDA HENEQUEN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |