MAUDE report
MAUDE report 1218
Malfunction · received Aug 25, 1992 · PHILLIPS MEDICAL SYSTEM NORTH AMERICA
Key facts
| MDR report key | 1218 |
|---|---|
| Report number | 1218 |
| Event type | Malfunction |
| Model number | 9874 227 07011 |
| Manufacturer | PHILLIPS MEDICAL SYSTEM NORTH AMERICA |
| Date received by FDA | Aug 25, 1992 |
| Report date | Aug 11, 1992 |
| Report source | Maude |
At a glance
- None Device problems coded
- No Adverse event flagged
- Yes Product problem flagged
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE medical device reports
MAUDE holds medical device reports (MDRs) of suspected device-associated deaths, serious injuries and malfunctions submitted to the FDA by manufacturers, importers, user facilities and the public. A report alone does not establish that a device caused an event.
Source: U.S. Food and Drug Administration (FDA), MAUDE (Manufacturer and User Facility Device Experience) database · Source date: