BIOPINCE Adverse Event — Malfunction (MDR MW5005571)
BIOPINCE Adverse Event — Malfunction (MDR MW5005571) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BIOPINCE; Generic name: BIOPSY GUN 18GAX15CM; Manufacturer: MEDICAL DEVICE TECHNOLOGIES INC..
| Device | BIOPINCE |
|---|---|
| Generic name | BIOPSY GUN 18GAX15CM |
| Manufacturer | MEDICAL DEVICE TECHNOLOGIES INC. |
| Report number | MW5005571 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-01-18 |
| Narrative | DURING A RENAL BIOPSY, WE HAD A BIOPINCE FULL CORE BIOPSY INSTRUMENT THAT WAS UNABLE TO BE COCKED AND USED. WE OPENED ANOTHER PACKAGE AND USED A DIFFERENT BIOPSY GUN. THE LOT NUMBER IS 73381KD5. THE MANUFACTURER IS MEDICAL DEVICE TECHNOLOGIES INC. DATE OF USE: ONE DAY IN 2008. DIAGNOSIS REASON FOR USE: ELEVATED CREATININE. |
| Source | openFDA MAUDE (device adverse events) |
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