UNSPECIFIED VACUTAINER BLOOD COLLECTION TUBE Adverse Event — Malfunction (MDR 2243072-2020-00671)
UNSPECIFIED VACUTAINER BLOOD COLLECTION TUBE Adverse Event — Malfunction (MDR 2243072-2020-00671) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNSPECIFIED VACUTAINER BLOOD COLLECTION TUBE; Generic name: UNSPECIFIED VACUTAINER BLOOD COLLECTION TUBE; Manufacturer: BECTON DICKIN
| Device | UNSPECIFIED VACUTAINER BLOOD COLLECTION TUBE |
|---|---|
| Generic name | UNSPECIFIED VACUTAINER BLOOD COLLECTION TUBE |
| Manufacturer | BECTON DICKINSON |
| Report number | 2243072-2020-00671 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | OTHER, USER FACILITY |
| 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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