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NIPRO HYPODERMIC NEEDLE - BULK Adverse Event — Malfunction (MDR 8041145-2020-00004)

NIPRO HYPODERMIC NEEDLE - BULK Adverse Event — Malfunction (MDR 8041145-2020-00004) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: NIPRO HYPODERMIC NEEDLE - BULK; Generic name: HYPODERMIC NEEDLE; Manufacturer: NIPRO (THAILAND) CORP. LTD..

DeviceNIPRO HYPODERMIC NEEDLE - BULK
Generic nameHYPODERMIC NEEDLE
ManufacturerNIPRO (THAILAND) CORP. LTD.
Report number8041145-2020-00004
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceDISTRIBUTOR
NarrativeSINCE THE CUSTOMER DID NOT RECORD THE LOT NUMBER FOR THE DEVICE IN QUESTION, INVESTIGATION REPORT IS ON RETAINED REPRESENTATIVE LOTS, BASED ON LOTS SHIPPED TO THE CUSTOMER.
SourceopenFDA MAUDE (device adverse events)

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