JAMSHIDI NEEDLE Adverse Event — Injury (MDR MW5005577)
JAMSHIDI NEEDLE Adverse Event — Injury (MDR MW5005577) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: JAMSHIDI NEEDLE; Generic name: JAMSHIDI NEEDLE; Manufacturer: CARDINAL HEALTH.
| Device | JAMSHIDI NEEDLE |
|---|---|
| Generic name | JAMSHIDI NEEDLE |
| Manufacturer | CARDINAL HEALTH |
| Report number | MW5005577 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-15 |
| Narrative | WHEN ATTEMPTING TO OBTAIN BONE BIOPSY ON PATIENT, BIOPSY NEEDLE BROKE OFF. DECISION WAS MADE BY PHYSICIANS TO NOT RETRIEVE NEEDLE. DATES OF USE: ONE DAY IN 2008. DIAGNOSIS OR REASON FOR URSE: SICKLE CELL ANEMIA. |
| Source | openFDA MAUDE (device adverse events) |
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