BD VACUTAINER® K2E 10.8MG PLUS BLOOD COLLECTION TUBES Adverse Event — Malfunction (MDR 9617032-2020-00370)
BD VACUTAINER® K2E 10.8MG PLUS BLOOD COLLECTION TUBES Adverse Event — Malfunction (MDR 9617032-2020-00370) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BD VACUTAINER® K2E 10.8MG PLUS BLOOD COLLECTION TUBES; Generic name: BLOOD SPECIMEN COLLECTION DEVICE; Manufacturer: BECTON,
| Device | BD VACUTAINER® K2E 10.8MG PLUS BLOOD COLLECTION TUBES |
|---|---|
| Generic name | BLOOD SPECIMEN COLLECTION DEVICE |
| Manufacturer | BECTON, DICKINSON AND COMPANY (BD) |
| Report number | 9617032-2020-00370 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | FOREIGN, OTHER, USER FACILITY |
| Narrative | DATE OF EVENT: UNKNOWN. THE DATE RECEIVED BY MANUFACTURER HAS BEEN USED FOR THIS FIELD. INITIAL REPORTER PHONE #: UNKNOWN. A SAMPLE IS AVAILABLE FOR EVALUATION. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED. |
| Source | openFDA MAUDE (device adverse events) |
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