MAUDE report
MAUDE report 4191: K-MODULE
Injury · received Jul 10, 1992 · BAXTER HEALTHCARE CORP PHARMASEAL
Key facts
| MDR report key | 4191 |
|---|---|
| Report number | 4191 |
| Event type | Injury |
| Brand name | K-MODULE |
| Model number | K-20 |
| Manufacturer | BAXTER HEALTHCARE CORP PHARMASEAL |
| Product code | LNG |
| Date received by FDA | Jul 10, 1992 |
| Report date | Jan 15, 1992 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1–9 MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- None 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: