PRECISION GLIDE NEEDLE 30G X 1/2 Adverse Event — Malfunction (MDR 10000339)
PRECISION GLIDE NEEDLE 30G X 1/2 Adverse Event — Malfunction (MDR 10000339) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PRECISION GLIDE NEEDLE 30G X 1/2; Generic name: NEEDLE, HYPODERMIC, SINGLE LUMEN; Manufacturer: BECTON DICKINSON AND COMPANY.
| Device | PRECISION GLIDE NEEDLE 30G X 1/2 |
|---|---|
| Generic name | NEEDLE, HYPODERMIC, SINGLE LUMEN |
| Manufacturer | BECTON DICKINSON AND COMPANY |
| Report number | 10000339 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Narrative | PER MD, "WHEN I OPENED ONE OF OUR SEALED BD 30 GAUGE HALF INCH NEEDLES THIS MORNING, I NOTICED BLACK MOLD INSIDE THE NEEDLE." DEVICE RETAINED AND WILL BE RETURNED TO THE MANUFACTURER. NO PATIENT HARM; DEVICE WAS IDENTIFIED PRIOR TO USE ON A PATIENT. |
| Source | openFDA MAUDE (device adverse events) |
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