MAUDE report
MAUDE report 8659: DOME PORT WITH ATTACHABLE GROSHONG CATHETER INTRODUCER
Malfunction · received Aug 11, 1994 · BARD ACESS SYSTEMS, INC.
Key facts
| MDR report key | 8659 |
|---|---|
| Report number | 8659 |
| Event type | Malfunction |
| Brand name | DOME PORT WITH ATTACHABLE GROSHONG CATHETER INTRODUCER |
| Model number | UNKNOWN |
| Catalog number | UNKNOWN |
| Manufacturer | BARD ACESS SYSTEMS, INC. |
| Product code | DYB |
| Device class | Class II |
| Date received by FDA | Aug 11, 1994 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ MAUDE reports for this product code
- 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: