FDA Adverse Event
Malfunction
Summary report: N
INION CPS BIOABSORBABLE SYSTEM
MDR report key: 514374
·
Received January 14, 2004
Report
- Report Number
- 9710629-2003-00004
- Event Type
- Malfunction
- Date Received
- January 14, 2004
- Date of Event
- September 3, 2003
- Report Date
- December 15, 2003
- Manufacturer
- INION LTD.
- Product Code
- HWC
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FI
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
ALIGNMENT OF TEETH/JAW PERFECT AFTER THE SURGERY. GUIDING ELDSTICS WERE APPLIED. ONE-DAY POSTOP ALIGNMENT OF TEETH/JAWS WAS NOTICED TO BE CHANGED. FIVE-WEEKS POSTOP X-RAYS SHOWED THAT THE PROXIMAL FRAGMENTS HAD ROTATED UPWARD. AT REOPERATION SCREWS WERE DETECTED TO BE BROKEN AND WERE REPLACED WITH STAINLESS STEEL SCREWS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INION CPS BIOABSORBABLE SYSTEM | BONE FIXATION FASTENER | HWC | INION LTD. | SCR-1216 | 0202027 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 37 YR | Required Intervention |