BD NEEDLE 27X1/2 LL ECLIPSE¿ Adverse Event — Malfunction (MDR 3003916417-2020-00128)
BD NEEDLE 27X1/2 LL ECLIPSE¿ Adverse Event — Malfunction (MDR 3003916417-2020-00128) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BD NEEDLE 27X1/2 LL ECLIPSE¿; Generic name: HYPODERMIC SINGLE LUMEN NEEDLE; Manufacturer: BECTON DICKINSON IND. CIRURGICAS LTDA.
| Device | BD NEEDLE 27X1/2 LL ECLIPSE¿ |
|---|---|
| Generic name | HYPODERMIC SINGLE LUMEN NEEDLE |
| Manufacturer | BECTON DICKINSON IND. CIRURGICAS LTDA |
| Report number | 3003916417-2020-00128 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | FOREIGN, OTHER |
| Narrative | IT WAS REPORTED THAT NEEDLE WAS CLOGGED DURING USE WITH A BD NEEDLE 27X1/2 LL ECLIPSE¿. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM PORTUGUESE TO ENGLISH: NEEDLE "CLOGGED", MAKING NOT POSSIBLE TO APPLY THE MEDICATION. |
| Source | openFDA MAUDE (device adverse events) |
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