FDA Adverse Event Malfunction Summary report: N

KYPHON XPANDER¿ II INFLATABLE BONE TAMP

MDR report key: 5509978 · Received March 18, 2016

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

Additional Manufacturer Narrative · 1

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.

Additional Manufacturer Narrative · 1

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.

Description of Event or Problem · 1

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