FDA Adverse Event
Injury
Summary report: N
GLOBAL SHD HYL PEG GLENOID 48
MDR report key: 376535
·
Received February 14, 2002
Report
- Report Number
- 1818910-2002-00073
- Event Type
- Injury
- Date Received
- February 14, 2002
- Report Date
- February 14, 2002
- Manufacturer
- DEPUY ORTHOPAEDICS, INC.
- Product Code
- KWS
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
THE PT WAS REVISED DUE TO POLY WEAR.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GLOBAL SHD HYL PEG GLENOID 48 | TOTAL SHOULDER PROSTHESIS | KWS | DEPUY ORTHOPAEDICS, INC. | NA | 783210 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 66 YR | Required Intervention |