MAUDE report
MAUDE report 9370: QUEST INFUSOR
Malfunction · received Jul 12, 1993 · KENDALL MCGAW LABORATORY
Key facts
| MDR report key | 9370 |
|---|---|
| Report number | 9370 |
| Event type | Malfunction |
| Brand name | QUEST INFUSOR |
| Model number | QUEST 2001 |
| Manufacturer | KENDALL MCGAW LABORATORY |
| Product code | KZD |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Jul 12, 1993 |
| Report date | Jun 28, 1993 |
| Report source | Maude |
At a glance
- None Device problems coded
- 100–999 MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- None Death reports for this brand
- None 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: