IMUFLEX BLOOD BAG SYSTEM Adverse Event — Malfunction (MDR 9681839-2020-00053)
IMUFLEX BLOOD BAG SYSTEM Adverse Event — Malfunction (MDR 9681839-2020-00053) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: IMUFLEX BLOOD BAG SYSTEM; Generic name: IMUFLEX WB-RP BLOOD BAG SYSTEM WITH LR FILTER; Manufacturer: TERUMO CORPORATION.
| Device | IMUFLEX BLOOD BAG SYSTEM |
|---|---|
| Generic name | IMUFLEX WB-RP BLOOD BAG SYSTEM WITH LR FILTER |
| Manufacturer | TERUMO CORPORATION |
| Report number | 9681839-2020-00053 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | INVESTIGATION IS IN PROCESS. A FOLLOW-UP REPORT WILL BE PROVIDED. |
| Source | openFDA MAUDE (device adverse events) |
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