LEVEL 1 HOTLINE BLOOD AND FLUID WARM Adverse Event — Malfunction (MDR 3012307300-2020-03393)
LEVEL 1 HOTLINE BLOOD AND FLUID WARM Adverse Event — Malfunction (MDR 3012307300-2020-03393) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: LEVEL 1 HOTLINE BLOOD AND FLUID WARM; Generic name: WARMER, THERMAL, INFUSION FLUID; Manufacturer: ST PAUL.
| Device | LEVEL 1 HOTLINE BLOOD AND FLUID WARM |
|---|---|
| Generic name | WARMER, THERMAL, INFUSION FLUID |
| Manufacturer | ST PAUL |
| Report number | 3012307300-2020-03393 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | USER FACILITY |
| Narrative | INFORMATION WAS RECEIVED INDICATING THAT A SMITHS MEDICAL LEVEL 1 HOTLINE BLOOD AND FLUID WARMER IS REPORTED TO BE LEAKING FROM THE GLASS. THERE WERE NO REPORTED ADVERSE EFFECTS. |
| Source | openFDA MAUDE (device adverse events) |
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