MAUDE report
MAUDE report 80025: JOHNSON & JOHNSON ARTICAULAR INSERT
Injury · received Mar 27, 1997 · JOHNSON & JOHNSON PROF, INC.
Key facts
| MDR report key | 80025 |
|---|---|
| Report number | 80025 |
| Event type | Injury |
| Brand name | JOHNSON & JOHNSON ARTICAULAR INSERT |
| Model number | 17.5MM |
| Catalog number | 866084 SIZE 5 (17.5MM) |
| Manufacturer | JOHNSON & JOHNSON PROF, INC. |
| Product code | HSH |
| Device class | Class II |
| Date received by FDA | Mar 27, 1997 |
| Report date | Mar 27, 1997 |
| 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: