PHILLIPS Adverse Event — Malfunction (MDR MW5005563)
PHILLIPS Adverse Event — Malfunction (MDR MW5005563) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PHILLIPS; Generic name: BP PATIENT MONITOR TUBING; Manufacturer: PHILLIPS.
| Device | PHILLIPS |
|---|---|
| Generic name | BP PATIENT MONITOR TUBING |
| Manufacturer | PHILLIPS |
| Report number | MW5005563 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Narrative | PATIENT REPORTS SUSTAINING LINEAR SUPERFICIAL ABRASIONS ON BILATERAL ARMS THAT SHE CLAIMS WERE CAUSED BY NEW BLOOD PRESSURE CUFF. TO BE USED ON PATIENT MONITORS. |
| Source | openFDA MAUDE (device adverse events) |
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