FDA Adverse Event
Malfunction
Summary report: N
10 LEAD ECG TRUNK AAMI/IEC 2M
MDR report key: 3945198
·
Received May 6, 2014
Report
- Report Number
- 9610816-2014-00114
- Event Type
- Malfunction
- Date Received
- May 6, 2014
- Report Date
- April 23, 2014
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Product Code
- DSA
- PMA / PMN Number
- K020531
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
(B)(4). A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THE FAILURE OF AN M1663A ECG TRUNK CABLE. THERE WAS NO REPORT OF PATIENT HARM.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 271196 | 10 LEAD ECG TRUNK AAMI/IEC 2M | DSA | PHILIPS MEDICAL SYSTEMS | M1663A | 2A |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |