BD ULTRA-FINE¿ NANO INSULIN PEN NEEDLE Adverse Event — Malfunction (MDR 9616656-2020-00364)

Name: BD ULTRA-FINE¿ NANO INSULIN PEN NEEDLE Adverse Event — Malfunction (MDR 9616656-2020-00364)
Creator: DeviceEvents

BD ULTRA-FINE¿ NANO INSULIN PEN NEEDLE Adverse Event — Malfunction (MDR 9616656-2020-00364) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BD ULTRA-FINE¿ NANO INSULIN PEN NEEDLE; Generic name: HYPODERMIC SINGLE LUMEN NEEDLE; Manufacturer: BECTON DICKINSON AND CO..

Device	BD ULTRA-FINE¿ NANO INSULIN PEN NEEDLE
Generic name	HYPODERMIC SINGLE LUMEN NEEDLE
Manufacturer	BECTON DICKINSON AND CO.
Report number	9616656-2020-00364
Event type	Malfunction
Product problem	Y
Date received	2020-04-27
Report source	CONSUMER, OTHER
Narrative	H.6. INVESTIGATION: NO SAMPLES (INCLUDING PHOTOS) WERE RETURNED AS OF (B)(6)2020 THEREFORE THE COMPLAINT COULD NOT BE CONFIRMED AND THE ROOT CAUSE IS UNDETERMINED. UNABLE TO PERFORM A DHR REVIEW DUE TO AN UNKNOWN LOT NUMBER. H3 OTHER TEXT : SEE H.10
Source	openFDA MAUDE (device adverse events)

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