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RADIATION STERILIZED EXTENSION SETS Adverse Event — Injury (MDR 1416980-2020-02415)

RADIATION STERILIZED EXTENSION SETS Adverse Event — Injury (MDR 1416980-2020-02415) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: RADIATION STERILIZED EXTENSION SETS; Generic name: SET, ADMINISTRATION, INTRAVASCULAR; Manufacturer: BAXTER HEALTHCARE CORPORATION.

DeviceRADIATION STERILIZED EXTENSION SETS
Generic nameSET, ADMINISTRATION, INTRAVASCULAR
ManufacturerBAXTER HEALTHCARE CORPORATION
Report number1416980-2020-02415
Event typeInjury
Product problemY
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE, HEALTH
NarrativeALTERNATE REPORTER PHONE NUMBER (CELL): (B)(6). DEVICE MANUFACTURER ADDRESS: (B)(4). SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
SourceopenFDA MAUDE (device adverse events)

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