MAUDE report
MAUDE report 927: SURGICAL SIMPLEX P RADIOPAQUE BONE CEMENT
Death · received Jul 23, 1992 · HOWMEDICA DIVISION, PFIZER HOSPITAL PRODUCTS GROUP, INC.
Key facts
| MDR report key | 927 |
|---|---|
| Report number | 927 |
| Event type | Death |
| Brand name | SURGICAL SIMPLEX P RADIOPAQUE BONE CEMENT |
| Model number | REZ 172 |
| Catalog number | 6191-1-001 |
| Manufacturer | HOWMEDICA DIVISION, PFIZER HOSPITAL PRODUCTS GROUP, INC. |
| Product code | LOD |
| Device class | Class II |
| Date received by FDA | Jul 23, 1992 |
| Report date | Jul 17, 1992 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ MAUDE reports for this product code
- 10–99 MAUDE reports for this brand
- 10–99 Death reports for this brand
- 1–9 Injury reports for this brand
- Yes Adverse event flagged
- No 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: