FDA Adverse Event
Injury
Summary report: N
MARQUETTE ELECTRONIC, INC.
MDR report key: 58397
·
Received December 27, 1996
Report
- Report Number
- 58397
- Event Type
- Injury
- Date Received
- December 27, 1996
- Date of Event
- December 4, 1996
- Report Date
- December 11, 1996
- Manufacturer
- MARQUETTE ELECTRONICS, INC.
- Product Code
- DRT
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- HI, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
EKG MONITOR DID NOT ALARM FOR ASYSTOLE. MONITOR REPORTED PAUSE. PT WAS PULSELESS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MARQUETTE ELECTRONIC, INC. | MONITORING SYSTEM | DRT | MARQUETTE ELECTRONICS, INC. | MODULAR CENTRAL SCOPE | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 62 YR | Life Threatening |