FDA Adverse Event
Injury
Summary report: N
SELF-COMPRESSION PLATE, 12 HOLE, 204MM
MDR report key: 22470
·
Received February 14, 1995
Report
- Report Number
- 1123762-1995-09001
- Event Type
- Injury
- Date Received
- February 14, 1995
- Date of Event
- January 12, 1995
- Report Date
- January 29, 1995
- Manufacturer
- ZIMMER, INC.
- Product Code
- HRS
- Product Problem
- Yes
- Report Source
- Distributor report
- Reporter Location
- VA, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
PT HAD BROKEN PLATE AND TWO SCREWS, PLATE AND SCREWS WERE REMOVED AND REPLACED WITH A ZMS INTRAMEDULLARY NAIL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SELF-COMPRESSION PLATE, 12 HOLE, 204MM Implant | SELF-COMPRESSION PLAE, 12 HOLE, 204MM | HRS | ZIMMER, INC. | NA | 59995300 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 74 YR | Hospitalization |