FDA Adverse Event
Injury
Summary report: N
INFINITY COLLARED TROCHANTERIC PRESS-FIT MODULE
MDR report key: 116669
·
Received August 29, 1997
Report
- Report Number
- 1043534-1997-00135
- Event Type
- Injury
- Date Received
- August 29, 1997
- Date of Event
- April 23, 1997
- Report Date
- May 27, 1997
- Manufacturer
- WRIGHT MEDICAL TECHNOLOGY, INC.
- Product Code
- JDI
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
CONCLUSION STATEMENT: THERE WAS NO DEVICE FAILURE. DEVICE WAS MANUFACTURED AND SOL BY DOW CORNING WRIGHT, WHO ASSETS WERE PURCHASED BY WRIGHT MEDICAL TECHNOLOGY, INC.
Description of Event or Problem · 1
REVISION SURGERY WAS PERFORMED FOR AN ALLEGEDLY BROKEN STEM. THIS COMPONENT WAS REVISED AT THAT TIME. NO COMPLAINT WAS STATED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INFINITY COLLARED TROCHANTERIC PRESS-FIT MODULE Implant | HIP COMPONENT - DEVICE 2 | JDI | WRIGHT MEDICAL TECHNOLOGY, INC. | NA | M692850 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NO INFO | Required Intervention |