MAUDE report
MAUDE report 16617: BECTON DICKINSON
Malfunction · received Mar 2, 1994 · BECTON DICKINSON VASCULAR ACCESS
Key facts
| MDR report key | 16617 |
|---|---|
| Report number | 16617 |
| Event type | Malfunction |
| Brand name | BECTON DICKINSON |
| Model number | 20 GUAGE 11/4 IN. 1.1MM |
| Catalog number | 3829591 3.2CM |
| Manufacturer | BECTON DICKINSON VASCULAR ACCESS |
| Date received by FDA | Mar 2, 1994 |
| Report date | Oct 26, 1993 |
| Report source | Maude |
At a glance
- None Device problems coded
- 100–999 MAUDE reports for this brand
- 1–9 Death reports for this brand
- 10–99 Injury reports for this brand
- 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: