Model Number 4100062000 |
Device Problem
Fracture (1260)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 06/29/2022 |
Event Type
malfunction
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Event Description
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The user facility reported that the device was breaking wires during a procedure.There was no patient involvement, no delay, no medical intervention, and no adverse consequences.
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Event Description
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The user facility reported that the device was breaking wires during a procedure.There was no patient involvement, no delay, no medical intervention, and no adverse consequences.
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Search Alerts/Recalls
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