FDA Adverse Event Injury Summary report: N

ACT 3-LEAD MCT

MDR report key: 13677676 · Received March 5, 2022

Report

Report Number
3027765-2022-00004
Event Type
Injury
Date Received
March 5, 2022
Date of Event
February 19, 2022
Report Date
March 5, 2022
Manufacturer
LIFEWATCH SERVICES, INC.
Product Code
DSI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 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. PER PATIENT USER GUIDE SUP546, PATIENTS ARE PROVIDED WARNING STATEMENTS REGARDING ELECTRODE SKIN IRRITATION. PATIENTS ARE INSTRUCTED TO CONTACT LIFEWATCH SERVICES CUSTOMER SUPPORT PRIOR TO USING THE MCT 3L MONITORING SYSTEM IF THEY HAVE KNOWN ALLERGIES TO NICKEL OR OTHER METALS. THE PATIENT IS ALSO INFORMED IN THE USER GUIDE THAT IF THEY DEVELOP SKIN IRRITATION THEY SHOULD CONTACT THEIR HEALTHCARE PROFESSIONAL. THE IFU LOCATED ON THE POUCH STATES THE ELECTRODES ARE HYPOALLERGENIC AND AN ELECTRODE IS TO BE WORN FOR LESS THAN 72 HOURS. THE ELECTRODES ARE ALSO PVC AND LATEX FREE. THE ELECTRODE SUPPLIER HAS NOT UNDERGONE CHANGES IN THE PRODUCTION PROCESS OR RAW MATERIALS AND MEET REQUIREMENTS FOR SKIN SENSITIVITY / CYTOTOXICITY / IRRITATION. NO ADDITIONAL INFORMATION IS KNOWN TO LIFEWATCH SERVICES, INC. AT THIS TIME.

Description of Event or Problem · 0

PATIENT COMMUNICATION OF CONSULTING A HEALTHCARE PROFESSIONAL DUE TO RASH AND ITCHY SKIN WHERE MEDICATION WAS PRESCRIBED (HYDROCORTISONE).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2569309 ACT 3-LEAD MCT SENSOR DSI LIFEWATCH SERVICES, INC. ACT 3-LEAD MCT UNAVAILABLE

Patients

Seq Age Sex Outcome Treatment
1 45 YR Female Other