BD VACUTAINER® K2E (EDTA) 7.2MG PLUS BLOOD COLLECTION TUBES Adverse Event — Malfunction (MDR 9617032-2020-00367)
BD VACUTAINER® K2E (EDTA) 7.2MG PLUS BLOOD COLLECTION TUBES Adverse Event — Malfunction (MDR 9617032-2020-00367) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BD VACUTAINER® K2E (EDTA) 7.2MG PLUS BLOOD COLLECTION TUBES; Generic name: BLOOD SPECIMEN COLLECTION DEVICE; Manufactu
| Device | BD VACUTAINER® K2E (EDTA) 7.2MG PLUS BLOOD COLLECTION TUBES |
|---|---|
| Generic name | BLOOD SPECIMEN COLLECTION DEVICE |
| Manufacturer | BECTON, DICKINSON AND COMPANY (BD) |
| Report number | 9617032-2020-00367 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN, OTHER, USER FACILITY |
| Narrative | IT WAS REPORTED AFTER USE THE BD VACUTAINER® K2E (EDTA) 7.2MG PLUS BLOOD COLLECTION TUBES HAD THE SHIELD/CAP/STOPPER DIFFERENT IN COLOR/SHADE/OR FADED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "A PROBLEM WITH THE COLOUR OF THE PURPLE CAP OF THE EDTA REFERENCE. SOME CAPS ARE LIGHTER THAN THE USUAL COLOR AND ARE THEREFORE MISLAID BY THE SORTING MACHINES. THIS MEANS THAT SOME T |
| Source | openFDA MAUDE (device adverse events) |
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