FDA Adverse Event
Injury
Summary report: N
BAK CAGES
MDR report key: 148015
·
Received January 9, 1998
Report
- Report Number
- 148015
- Event Type
- Injury
- Date Received
- January 9, 1998
- Date of Event
- November 19, 1997
- Report Date
- December 29, 1997
- Manufacturer
- ALLIED ORTHOPEDIC ASSOC.
- Product Code
- MAX
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- DE, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
CAGE LOST IN PERINEUM, RESULTING IN EXTENDED SURGERY AND BLOOD LOSS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BAK CAGES | SPINE STABILIZER | MAX | ALLIED ORTHOPEDIC ASSOC. | UNK | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 26 YR | Required Intervention |