inforMED
MalfunctionFSO

M822 F40

Received Jul 18, 2025 · Event occurred Jul 9, 2025

Report 3003974370-2025-00007 · MDR key 22541735

Device

Generic name

Surgical Microscope

Model number

10448142

Product problems

  • Unintended Electrical Shock
  • Unintended Electrical Shock

Patient

NA · Unknown

  • Electric Shock
  • Electric Shock

Narrative

Additional Manufacturer Narrative

THIS IS A FINAL REPORT. AN ON-SITE INVESTIGATION WAS PERFORMED BY THE FIELD SERVICE ENGINEER. INITIAL ASSESSMENT INDICATES POSSIBLE POWER OR GROUNDING FAULTS THAT REQUIRE FURTHER INVESTIGATION. A WIRING FAULT IS SUSPECTED IN THE OTTOFLEX LAMP. IN HEAVILY USED DEVICES, THE POWER CABLES TO THE BULB CAN BREAK, CAUSING INTERMITTENT SHORTS AND LIGHT FAILURE. THE POSSIBILITY OF A DEFECTIVE LAMP CHANGER, WHICH COULD INTERMITTENTLY DISRUPT THE POWER TO THE BULB, WAS RAISED. A REMOTE DIAGNOSTIC SESSION WAS COORDINATED WITH THE GLOBAL SERVICE SUPPORT TEAM. DIAGNOSTIC TOOLS INCLUDED A MULTIMETER AND ELECTRICAL SAFETY TESTER. THE SAFETY TEST RESULTS DID NOT CONCLUSIVELY IDENTIFY A FAULT. NO PARTS WERE REPLACED; IT WAS ASSUMED THAT A BARE CABLE HAD BEEN RE-INSULATED RATHER THAN EXCHANGED. THE INTERNAL CAUSE WAS DOCUMENTED AS "BLANK SHEARED CABLE", INDICATING A DAMAGED OR EXPOSED WIRE THAT MAY HAVE CAUSED THE SHOCK. THE AFFECTED DEVICE IS OVER FOUR YEARS OLD AND HEAVILY USED. POSSIBLE WEAR OF THE CABLE INSULATION, RESULTING IN EXPOSED WIRE POTENTIAL, MAY HAVE CAUSED THE ELECTRIC SHOCK. A REVIEW OF THE DHR AND HIPOT TEST REPORT FOR THIS DEVICE REVEALED THAT THE DEVICE PASSED THE HIPOT TEST, INCLUDING THE LEAKAGE CURRENT TEST BEFORE IT WAS RELEASED FOR SHIPMENT. A REVIEW OF THE MANUFACTURING AND SERVICE RECORDS DID NOT REVEAL ANY EXPLANATION FOR THE INCIDENT. A REVIEW OF THE COMPLAINT STATISTICS DID NOT SHOW SIMILAR OR IDENTICAL CASES. THE REPORTED MALFUNCTION IS CONSIDERED AN ISOLATED EVENT AND DOES NOT INDICATE A DESIGN OR MANUFACTURING ISSUE. IT WAS REPORTED THAT THE ABOVE-MENTIONED CABLE WAS RE-INSULATED. AFTER RE-INSULATION, THE DEVICE WAS TESTED IN ACCORDANCE WITH RELEASED SERVICE PROCEDURES. THE DEVICE WORKS AS EXPECTED, AND THE MOST LIKELY ROOT CAUSE OF THE INCIDENT HAS BEEN CORRECTED. ADDITIONAL INFORMATION: IN THE INITIAL REPORT, THE CONTACT NAME OF THE INITIAL REPORTER WAS UNKNOWN; SEE SECTION E.1. BY THE TIME THIS FINAL REPORT WAS SUBMITTED, WE HAD NOT RECEIVED THE NAME OF THE CONTACT PERSON, DESPITE REPEATED REQUESTS. THEREFORE, WE ARE UNABLE TO PROVIDE THE MISSING INFORMATION.

Description of Event or Problem

LEICA MICROSYSTEMS (SCHWEIZ) AG RECEIVED A COMPLAINT FROM GREECE STATING THAT A NURSE SUFFERED AN ELECTRIC SHOCK WHILE TRANSPORTING AN M822 F40 FROM THE STORAGE ROOM TO THE OPERATING ROOM. NO INJURIES OCCURRED. SHE DESCRIBED HER ARM AS FEELING NUMB FOR A FEW SECONDS. NO MEDICAL INTERVENTION WAS REQUIRED. THERE WAS NO PATIENT INVOLVEMENT.

Additional Manufacturer Narrative

AN INVESTIGATION OF THE INCIDENT IS CURRENTLY UNDERWAY AND A FOLLOW-UP WILL BE SUBMITTED SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE FOLLOWING INVESTIGATION.