KYPHON XPANDER¿ II INFLATABLE BONE TAMP
Report
- Report Number
- 2953769-2016-00025
- Event Type
- Malfunction
- Date Received
- March 18, 2016
- Date of Event
- February 17, 2016
- Report Date
- April 12, 2016
- Manufacturer
- MDT KYPHON NEUCHATEL MFG
- Product Code
- HRX
- PMA / PMN Number
- K101864
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- PHYSICIAN
Narratives
ADDRESS: (B)(6). (B)(4). NEITHER THE DEVICE NOR FILMS OF APPLICABLE IMAGING STUDIES WERE RETURNED TO THE MANUFACTURER FOR EVALUATION. THEREFORE, WE ARE UNABLE TO DETERMINE THE DEFINITIVE CAUSE OF THE REPORTED EVENT.
ANALYSIS: DURING VISUAL ANALYSIS, NO PROBLEM HAS BEEN DETECTED ON THE IBT. DURING FUNCTIONAL ANALYSIS, THE IBT WAS UNABLE TO MAINTAINED PRESSURE, PROBABLY DUE TO A HOLE. AFTER FURTHER ANALYSIS, THE HOLE WAS CONFIRMED AND LOCATED BETWEEN THE TWO PEAK OF THE BALLOON THIS IS A VERY SMALL HOLE WHERE WATER IS SPRAYING WHEN UNDER PRESSURE. CONCLUSION: BASED ON THE INFORMATION PROVIDED, VISUAL AND FUNCTIONAL ANALYSIS, THE MOST PROBABLE ROOT CAUSE OF THE RUPTURE OF THE BALLOON IS ATTRIBUTED TO THE CONTACT WITH BONE SPLINTERS DURING SURGERY. A GOOD FAITH EFFORT WILL BE MADE TO OBTAIN THE APPLICABLE INFORMATION RELEVANT TO THE REPORT. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
PRE-OP DIAGNOSIS: "BWK 12" FRACTURE LEVELS IMPLANTED: "BWK 12" IT WAS REPORTED THAT ON (B)(6) 2016, INTRA-OP, BOTH BALLOONS RUPTURED IN THE VERTREBRAE BODY, DURING THE BKP EVENT. PRODUCT CAME IN CONTACT WITH THE PATIENT. NO PATIENT COMPLICATIONS WERE REPORTED TO THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 166323 | KYPHON XPANDER¿ II INFLATABLE BONE TAMP | ARTHROSCOPE | HRX | MDT KYPHON NEUCHATEL MFG | NA | 0007760074 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 00075 YR |