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. |