FDA Adverse Event Injury Summary report: N

NISSHA MEDICAL TECHNOLOGIES

MDR report key: 14042240 · Received April 7, 2022

Report

Report Number
1317188-2022-00007
Event Type
Injury
Date Received
April 7, 2022
Date of Event
February 19, 2022
Report Date
March 5, 2022
Manufacturer
MEDICO ELECTRODES INTERNATIONAL LTD
Product Code
DRX
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
PA, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

MEDICO WAS EMAILED FOR THEIR BIOCOMPATIBILITY REPORT. THE RESULTS OF THE GEL AND ADHESIVE (THOSE WHICH HAVE DIRECT CONTACT WITH SKIN) WERE BOTH FOUND TO BE NON-CYTOTOXIC, NON-SENSITIZING, AND NON-IRRITATING. MEDICO ALSO STATES THEY USED APPROVED SUPPLIERS THAT FOLLOW STANDARDIZED QMS AND ALL RAW MATERIALS ARE INSPECTED WHEN RECEIVED IN. SEE ATTACHMENTS. MEDICO HAS STATED THAT AFTER REVIEW OF THEIR RAW MATERIAL AND PRODUCTION RECORDS, THERE WERE NO CHANGES TO THE COMPOSITION OF THE RAW MATERIALS AND NO CHANGES IN PRODUCTION. A TREND REPORT SHOWS THERE HAS NOT BEEN A SIGNIFICANT INCREASE IN SKIN REACTION COMPLAINTS OVER THE PAST 3 YEARS AND THE ELECTRODES ARE SOLD WORLDWIDE. THE IFU (ON THE POUCH) STATES THE ELECTRODES ARE HYPOALLERGENIC AND AN ELECTRODE IS ONLY TO BE WORN FOR LESS THAN 72 HOURS. AS A LOT NUMBER WAS NOT PROVIDED, A REVIEW OF LOT RECORD PAPERWORK CANNOT BE COMPLETED.

Description of Event or Problem · 0

THE PATIENT CONSULTED A CLINICIAN AND PRESENTED WITH A RASH AND SKIN ITCH. THE PHYSICIAN PRESCRIBED HYDROCORTISONE TO APPLY TO THE AFFECTED AREA. THE PATIENT WAS PROVIDED WITH A DIFFERENT TYPE OF ELECTRODE TO CONTINUE ENROLLMENT. THE PATIENT DID ADVISE THEY HAVE SENSITIVE SKIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1695124 NISSHA MEDICAL TECHNOLOGIES ECG MONITORING ELECTRODE DRX MEDICO ELECTRODES INTERNATIONAL LTD A10091-30 UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 45 YR Female Other