FDA Adverse Event Malfunction Summary report: N

HAND PIECE FOR BATTERY POWERED DRIVER

MDR report key: 20453076 · Received October 15, 2024

Report

Report Number
8030965-2024-12844
Event Type
Malfunction
Date Received
October 15, 2024
Manufacturer
SYNTHES GMBH
Product Code
HWE
UDI-DI
7611819890084
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THIS REPORT IS BEING SUBMITTED PURSUANT TO THE PROVISIONS OF 21 CFR, PART 803 (AND/OR PART 4, AS APPLICABLE). THIS REPORT MAY BE BASED ON INFORMATION WHICH HAS NOT BEEN INVESTIGATED OR VERIFIED PRIOR TO THE REQUIRED REPORTING DATE. THIS REPORT DOES NOT REFLECT A CONCLUSION BY DEPUY SYNTHES, OR ITS EMPLOYEES THAT THE REPORT CONSTITUTES AN ADMISSION THAT THE PRODUCT, DEPUY SYNTHES, OR ITS EMPLOYEES CAUSED OR CONTRIBUTED TO THE POTENTIAL EVENT DESCRIBED IN THIS REPORT. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL REPORT, A FOLLOW-UP REPORT WILL BE FILED AS APPROPRIATE. ADDITIONAL NARRATIVE: SERVICE AND REPAIR EVALUATION: THE CUSTOMER REPORTED THAT THE HAND PIECE FOR BATTERY POWERED DRIVER WILL NOT TURN ON. THE ISSUE WAS OBSERVED DURING TESTING. THE REPAIR TECHNICIAN REPORTED DAMAGED VENT, DEVICE DID NOT RUN IN FORWARD, FAST FORWARD AND REVERSE CONDITION, DISCOLORED WIRES, DEBRIS ON BARRIERS, DAMAGED DRIVE COLUMN, MELTED CONTACT PLATE ON INSIDE. THE CAUSE OF THE ISSUE IS FAULTY PARTS. THE ITEM WILL BE REPAIRED, PUT THROUGH FINAL INSPECTION, AND WILL BE RETURNED TO THE CUSTOMER UPON COMPLETION OF THE SERVICE AND REPAIR PROCESS. THE EVALUATION WAS CONFIRMED. THE DEVICE WAS DEEMED SERVICEABLE AND WILL BE RETURNED TO THE CUSTOMER, NO DESIGN OR MANUFACTURING ISSUES WERE IDENTIFIED THEREFORE IT HAS BEEN DETERMINED THAT NO CORRECTIVE AND/OR PREVENTATIVE ACTION IS PROPOSED. DEVICE HISTORY RECORD (DHR) REVIEW CONDUCTED: PART # 05.000.008 SYNTHES LOT # 003577 SUPPLIER LOT # 003577 RELEASE TO WAREHOUSE DATE: 09 JULY 2010 SUPPLIER: TRIANGLE MANUFACTURING NO NCRS WERE GENERATED DURING PRODUCTION. REVIEW OF THE DEVICE HISTORY RECORD(S) SHOWED THAT THERE WERE NO ISSUES DURING THE MANUFACTURE OF THIS PRODUCT, AND ANY SUB-COMPONENTS, WHICH WOULD CONTRIBUTE TO THIS COMPLAINT CONDITION.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE HAND PIECE FOR BATTERY POWERED DRIVER WILL NOT TURN ON. THE ISSUE WAS OBSERVED DURING TESTING. NO INJURIES, NO DELAYS. THERE WAS NO PATIENT INVOLVEMENT. NO FURTHER INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
319723 HAND PIECE FOR BATTERY POWERED DRIVER INSTR,SURGICAL,ORTHOPEDIC,AC- POWERED MOTOR/ACCESS & ATTACH HWE SYNTHES GMBH 003577 7611819890084

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown