MAUDE report
MAUDE report 75380: PALL RCXL1 LEUKOCYTE REDUCTION FILTER FOR RED CELL TRANS
No Answer Provided · received Mar 12, 1997 · PALL BIOMEDICAL PRODUCTS CO.
Key facts
| MDR report key | 75380 |
|---|---|
| Report number | 2432733-1997-00011 |
| Event type | No Answer Provided |
| Brand name | PALL RCXL1 LEUKOCYTE REDUCTION FILTER FOR RED CELL TRANS |
| Model number | RCXL1KLE |
| Manufacturer | PALL BIOMEDICAL PRODUCTS CO. |
| Product code | CAK |
| Device class | Class II |
| Date received by FDA | Mar 12, 1997 |
| Report date | Feb 10, 1997 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ 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: