UNSPECIFIED BD SYRINGE Adverse Event — Malfunction (MDR 2243072-2020-00669)
UNSPECIFIED BD SYRINGE Adverse Event — Malfunction (MDR 2243072-2020-00669) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNSPECIFIED BD SYRINGE; Generic name: PISTON SYRINGE; Manufacturer: BECTON DICKINSON.
| Device | UNSPECIFIED BD SYRINGE |
|---|---|
| Generic name | PISTON SYRINGE |
| Manufacturer | BECTON DICKINSON |
| Report number | 2243072-2020-00669 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER, OTHER |
| Narrative | UNKNOWN MANUFACTURER: THERE ARE MULTIPLE BD LOCATIONS WHERE THIS UNSPECIFIED BD DEVICE MAY HAVE BEEN MANUFACTURED. A CATALOG AND LOT NUMBER COULD NOT BE CONFIRMED FOR THIS INCIDENT AND WITHOUT THIS INFORMATION WE ARE UNABLE TO DETERMINE WHERE THE DEVICE WAS MANUFACTURED. THEREFORE, BD CORPORATE HEADQUARTERS IN (B)(4) HAS BEEN LISTED AND THE (B)(4) FDA REGISTRATION NUMBER HAS BEEN USED FOR THE MANU |
| Source | openFDA MAUDE (device adverse events) |
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