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NEEDLE 27X1/2 LL ECLIPSE Adverse Event — Malfunction (MDR 3003916417-2020-00126)

NEEDLE 27X1/2 LL ECLIPSE Adverse Event — Malfunction (MDR 3003916417-2020-00126) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: NEEDLE 27X1/2 LL ECLIPSE; Generic name: NEEDLE; Manufacturer: BECTON DICKINSON IND. CIRURGICAS LTDA.

DeviceNEEDLE 27X1/2 LL ECLIPSE
Generic nameNEEDLE
ManufacturerBECTON DICKINSON IND. CIRURGICAS LTDA
Report number3003916417-2020-00126
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceFOREIGN, OTHER, USER FACILITY
NarrativeIT WAS REPORTED THAT NEEDLE 27X1/2 LL ECLIPSE WAS CLOGGED DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CLOGGED NEEDLE.
SourceopenFDA MAUDE (device adverse events)

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