CL CATHETER EXT SET/LUER ACT. VALVE MLL ADAPTER Adverse Event — Injury (MDR 6000001-2008-00058)
CL CATHETER EXT SET/LUER ACT. VALVE MLL ADAPTER Adverse Event — Injury (MDR 6000001-2008-00058) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CL CATHETER EXT SET/LUER ACT. VALVE MLL ADAPTER; Generic name: 80FPA; Manufacturer: BAXTER HEALTHCARE CORP..
| Device | CL CATHETER EXT SET/LUER ACT. VALVE MLL ADAPTER |
|---|---|
| Generic name | 80FPA |
| Manufacturer | BAXTER HEALTHCARE CORP. |
| Report number | 6000001-2008-00058 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-19 |
| Report source | Health Professional, User facility |
| Narrative | A FACILITY REPORTED THAT A FEMALE ADULT PATIENT WHO HAD USED THE CLEARLINK EXTENSION SET DURING AN INITIAL HOSPITALIZATION, WAS DISCHARGED AND RETURNED A FEW DAYS LATER FOR A SECOND ADMISSION BECAUSE THE INTRAVENOUS (IV) SITE HAD BECOME NECROTIC AND REQUIRED CHEMICAL DEBRIDEMENT. |
| Source | openFDA MAUDE (device adverse events) |
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