RELIAVAC 400 EVACUATOR, 400ML CAPACITY, Y-CONNECTING TUBE, 35" STERILE Adverse Event — Malfunction (MDR 1018233-2020-02893)
RELIAVAC 400 EVACUATOR, 400ML CAPACITY, Y-CONNECTING TUBE, 35" STERILE Adverse Event — Malfunction (MDR 1018233-2020-02893) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: RELIAVAC 400 EVACUATOR, 400ML CAPACITY, Y-CONNECTING TUBE, 35" STERILE; Generic name: SUCTION EVACUATOR; Ma
| Device | RELIAVAC 400 EVACUATOR, 400ML CAPACITY, Y-CONNECTING TUBE, 35" STERILE |
|---|---|
| Generic name | SUCTION EVACUATOR |
| Manufacturer | C.R. BARD, INC. (COVINGTON) -1018233 |
| Report number | 1018233-2020-02893 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | DISTRIBUTOR, OTHER |
| Narrative | IT WAS REPORTED THAT IT WAS DIFFICULT TO INFLATE THE SUCTION EVACUATOR DURING PRETEST. |
| Source | openFDA MAUDE (device adverse events) |
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