BD ULTRA-FINE¿ NANO¿ PEN NEEDLES 4MM (5/32¿) 32G Adverse Event — Injury (MDR 9616656-2020-00367)
BD ULTRA-FINE¿ NANO¿ PEN NEEDLES 4MM (5/32¿) 32G Adverse Event — Injury (MDR 9616656-2020-00367) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BD ULTRA-FINE¿ NANO¿ PEN NEEDLES 4MM (5/32¿) 32G; Generic name: HYPODERMIC SINGLE LUMEN NEEDLE; Manufacturer: BECTON DICKINSON AND CO.
| Device | BD ULTRA-FINE¿ NANO¿ PEN NEEDLES 4MM (5/32¿) 32G |
|---|---|
| Generic name | HYPODERMIC SINGLE LUMEN NEEDLE |
| Manufacturer | BECTON DICKINSON AND CO. |
| Report number | 9616656-2020-00367 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER, OTHER |
| Narrative | IT WAS REPORTED THAT 4 BD ULTRA-FINE¿ NANO¿ PEN NEEDLES 4MM (5/32¿) 32G EXPERIENCED DIFFICULTY OPERATING OR NOT WORKING/FUNCTIONING, LEAKAGE, AN INABILITY OR DIFFICULTY PRIMING, AND AN INABILITY TO DELIVER INSULIN/MEDICATION. PRODUCT DEFECTS WERE NOTED DURING USE. THE DEVICES WERE ALSO INVOLVED IN A SERIOUS INJURY IN THE FORM OF HYPERGLYCEMIA. PATIENT EXPERIENCED HYPERGLYCEMIA AS A RESULT OF THE D |
| Source | openFDA MAUDE (device adverse events) |
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