NIPRO HYPODERMIC NEEDLE - BULK Adverse Event — Malfunction (MDR 1056186-2020-00004)
NIPRO HYPODERMIC NEEDLE - BULK Adverse Event — Malfunction (MDR 1056186-2020-00004) 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..
| Device | NIPRO HYPODERMIC NEEDLE - BULK |
|---|---|
| Generic name | HYPODERMIC NEEDLE |
| Manufacturer | NIPRO (THAILAND) CORP. LTD. |
| Report number | 1056186-2020-00004 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Narrative | NEEDLE BROKE OFF WHILE INJECTING INTO PATIENT. ADDITIONAL INFORMATION 04/03/20: DURING PERMANENT PACING PROCEDURE, THE PHYSICIAN WAS INJECTING LIDOCAINE INTO THE PATIENT, THE NEEDLE BROKE OFF AND ULTIMATELY RETRIEVED FROM THE PATIENT USING FORCEPS. THERE WAS NO REPORT OF MEDICAL INTERVENTION OR SERIOUS INJURY REPORTED RELATED TO THIS INCIDENT. NO ADDITIONAL INFORMATION IS AVAILABLE. POSSIBLE LOT N |
| Source | openFDA MAUDE (device adverse events) |
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