FDA Adverse Event Injury Summary report: N

ACUITY CENTRAL STATION

MDR report key: 398563 · Received June 6, 2002

Report

Report Number
3023750-2002-00003
Event Type
Injury
Date Received
June 6, 2002
Report Date
May 6, 2002
Manufacturer
WELCH ALLYN PROTOCOL, INC.
Product Code
DRT
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

CUSTOMER STATED THAT A PATIENT REQUIRED RESUSCITATION DURING AN INTERRUPTION OF MONITORING WITH A TELEMETRY DEVICE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ACUITY CENTRAL STATION CARDIAC MONITOR DRT WELCH ALLYN PROTOCOL, INC. ACUITY STATION NA

Patients

Seq Age Sex Outcome Treatment
1 NO INFO Life Threatening| O VHF TRANSMITTER P/N 100-0076-00.