FDA Adverse Event
Injury
Summary report: N
INFLAT-O-MATIC 3000
MDR report key: 119497
·
Received September 10, 1997
Report
- Report Number
- 1526350-1997-00023
- Event Type
- Injury
- Date Received
- September 10, 1997
- Report Date
- August 13, 1997
- Manufacturer
- ZIMMER PATIENT CARE DIVISION
- Product Code
- KCY
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IN, US
- Reporter Occupation
- ATTORNEY
Narratives
Description of Event or Problem · 1
A PT WAS ALLEGEDLY INJURED BY INFLAT-O-MATIC 3000 TOURNIQUET.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INFLAT-O-MATIC 3000 | PNEUMATIC TOURNIQUET SYSTEM | KCY | ZIMMER PATIENT CARE DIVISION | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NO INFO | Other |