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BD VACUTAINER® NH 68 I.U. PLUS BLOOD COLLECTION TUBES Adverse Event — Malfunction (MDR 9617032-2020-00364)

BD VACUTAINER® NH 68 I.U. PLUS BLOOD COLLECTION TUBES Adverse Event — Malfunction (MDR 9617032-2020-00364) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BD VACUTAINER® NH 68 I.U. PLUS BLOOD COLLECTION TUBES; Generic name: BLOOD SPECIMEN COLLECTION DEVICE; Manufacturer: BECTON,

DeviceBD VACUTAINER® NH 68 I.U. PLUS BLOOD COLLECTION TUBES
Generic nameBLOOD SPECIMEN COLLECTION DEVICE
ManufacturerBECTON, DICKINSON AND COMPANY (BD)
Report number9617032-2020-00364
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceFOREIGN, OTHER, USER FACILITY
NarrativeINITIAL REPORTER PHONE #: UNKNOWN. A DEVICE EVALUATION IS ANTICIPATED, BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.
SourceopenFDA MAUDE (device adverse events)

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