FDA Adverse Event
Injury
Summary report: N
DU PLASTER BDG XFST
MDR report key: 298300
·
Received September 28, 2000
Report
- Report Number
- 1624487-2000-00003
- Event Type
- Injury
- Date Received
- September 28, 2000
- Date of Event
- August 30, 2000
- Report Date
- September 27, 2000
- Manufacturer
- DEROYAL
- Product Code
- LGF
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AL, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
A CARAPACE PRODUCT, (UNABLE TO CONFIRM PRODUCT NUMBER), AFTER BEING WET DOWN WITH EXTREMELY HOT WATER WAS PLACED ON PTS LEG. PT COMPLAINED OF GREAT PAIN FAR IN EXCESS OF THE PAIN FROM PT'S BROKEN LEG, BUT WAS TRANSFERRED TO ANOTHER FACILITY APPROXIMATELY AN HOUR AWAY. WHEN CAST WAS REMOVED AT THIS FACILITY, PT HAD 2ND AND 3RD DEGREE BURNS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DU PLASTER BDG XFST | PLASTER BANDAGE | LGF | DEROYAL | NA | UNK. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN |