NISSHA MEDICAL TECHNOLOGIES
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
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.
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 |