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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.

DeviceJAMSHIDI NEEDLE
Generic nameJAMSHIDI NEEDLE
ManufacturerCARDINAL HEALTH
Report numberMW5005577
Event typeInjury
Product problemN
Date received2008-02-15
NarrativeWHEN 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.
SourceopenFDA MAUDE (device adverse events)

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