BD PRECISIONGLIDE¿ NEEDLE Adverse Event — Malfunction (MDR 1911916-2020-00417)
BD PRECISIONGLIDE¿ NEEDLE Adverse Event — Malfunction (MDR 1911916-2020-00417) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BD PRECISIONGLIDE¿ NEEDLE; Generic name: HYPODERMIC SINGLE LUMEN NEEDLE; Manufacturer: BD MEDICAL (BD WEST) MEDICAL SURGICAL.
| Device | BD PRECISIONGLIDE¿ NEEDLE |
|---|---|
| Generic name | HYPODERMIC SINGLE LUMEN NEEDLE |
| Manufacturer | BD MEDICAL (BD WEST) MEDICAL SURGICAL |
| Report number | 1911916-2020-00417 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN, OTHER, USER FACILITY |
| Narrative | INVESTIGATION SUMMARY: NO SAMPLE WAS RECEIVED. FOUR PHOTOS WERE PROVIDED. IT LOOKS THAT WERE TAKEN WITH A 100X MAGNIFICATION. 2 OF THE PHOTOS SHOW A NEEDLE WITH A HOOK, ONE PHOTO SHOWS A NEEDLE WITH A POINT NOT FULLY COMPLETE (FLAT). ANOTHER SHOWING THE INNER BOTTOM PART OF THE NEEDLE HUB. A DEVICE HISTORY RECORD REVIEW WAS COMPLETED WITH ZERO DEFECTS FOUND. NO QUALITY NOTIFICATIONS WERE WRITTEN F |
| Source | openFDA MAUDE (device adverse events) |
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