NEEDLE 30X1/2 RB Adverse Event — Malfunction (MDR 1911916-2020-00414)
NEEDLE 30X1/2 RB Adverse Event — Malfunction (MDR 1911916-2020-00414) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: NEEDLE 30X1/2 RB; Generic name: HYPODERMIC SINGLE LUMEN NEEDLE; Manufacturer: BD MEDICAL (BD WEST) MEDICAL SURGICAL.
| Device | NEEDLE 30X1/2 RB |
|---|---|
| Generic name | HYPODERMIC SINGLE LUMEN NEEDLE |
| Manufacturer | BD MEDICAL (BD WEST) MEDICAL SURGICAL |
| Report number | 1911916-2020-00414 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | DISTRIBUTOR, OTHER |
| Narrative | DEVICE EXPIRATION DATE: NA. INVESTIGATION SUMMARY: NO SAMPLES WERE RECEIVED. NO PHOTO WAS PROVIDED. THIS BATCH WAS PRODUCED DURING 2013. AT THAT TIME, THE EXPIRATION DATE WAS NOT A REQUIREMENT FOR BOX LABELS. NOTE: THIS PRODUCT¿S SHELF LIFE HAS EXPIRED. COMPLAINTS RECEIVED FOR THIS DEVICE AND REPORTED CONDITION WILL CONTINUE TO BE TRACKED AND TRENDED. INFORMATION WILL BE CAPTURED ON TREND REPORTS |
| Source | openFDA MAUDE (device adverse events) |
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