NMT CABLE
Received Nov 17, 2025 · Event occurred Nov 11, 2025
Report 9610816-2025-001072 · MDR key 23568580
Device
Generic name
Stimulator, Nerve, Peripheral, Electric
Manufacturer
Philips Medizin Systeme Böblingen GmbhModel number
INTELLIVUE NMT PATIENT CABLECatalog number
989803174581
Lot number
0123
Product problems
- Adverse Event Without Identified Device or Use Problem
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- Partial thickness (Second Degree) Burn
- Partial thickness (Second Degree) Burn
Narrative
Additional Manufacturer Narrative
ADDITIONAL INFORMATION WAS RECEIVED. THE ADDITIONAL INFORMATION WAS REVIEWED. IT WAS REPORTED THAT WHEN REMOVING THE PAD AFTER USE DURING THE OPERATION THE ISSUE WAS NOTICED. IT IS NOTED THAT THIS ORIGINATED FROM THE RED LEAD. THE BURN WAS DESCRIBED AS SEVERE REDNESS AND A SMALL BURN. THE BURN WAS TREATED WITH OINTMENT, OBSERVED FOR A COUPLE OF DAYS, NO BLISTERS, RESOLVED SPONTANEOUSLY. THE OINTMENT THE PATIENT WAS TREATED WITH IS CONSIDERED FIRST AID OVER THE COUNTER AND DOES NOT MEET THE CRITERIA FOR MEDICAL INTERVENTION. PER THE RESPONSE, NO PERMANENT DAMAGE, NO FURTHER ACTION TAKEN. THE NEW INFORMATION PROVIDED CLARIFIES THE INJURY. THIS BURN MEETS THE CRITERIA FOR A NON-SERIOUS MINOR INJURY. THIS IS NO LONGER CONSIDERED A REPORTABLE COMPLAINT WITH PHILIPS.
Additional Manufacturer Narrative
PHILIPS IS IN THE PROCESS OF OBTAINING ADDITIONAL INFORMATION CONCERNING THIS EVENT AND THE COMPLAINT IS STILL UNDER INVESTIGATION. A FINAL REPORT WILL BE SUBMITTED ONCE THE INVESTIGATION IS COMPLETE.
Description of Event or Problem
IT WAS REPORTED A PATIENT HAD SUFFERED FROM BURNS AFTER BEING MONITORED BY NEUROMUSCULAR TRANSMISSION (NMT) EQUIPMENT. NO OTHER CLINICAL INFORMATION OR MEDICAL INTERVENTION WAS REPORTED; THEREFORE, GOOD FAITH EFFORTS ARE BEING PERFORMED.