FDA Adverse Event
Other
Summary report: N
MCS METATARSAL COMPRESSION 45
MDR report key: 492123
·
Received October 24, 2003
Report
- Report Number
- 8010177-2003-00022
- Event Type
- Other
- Date Received
- October 24, 2003
- Date of Event
- October 1, 2003
- Report Date
- October 24, 2003
- Manufacturer
- STRYKER INSTRUMENTS
- Product Code
- JEY
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
PLATE HAD TO BE REMOVED POST-OP DUE TO PATIENT REACTION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MCS METATARSAL COMPRESSION 45 | BONE PLATE | JEY | STRYKER INSTRUMENTS | 6514-3-145 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 50 YR | Required Intervention |