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 04/28/2021 |
Event Type
malfunction
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Event Description
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The user facility reported that the device broke a wire during testing prior to 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 broke a wire during testing prior to a procedure. there was no patient involvement, no delay, no medical intervention, and no adverse consequences.
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Manufacturer Narrative
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Correction: d9; h3.Additional info h6.
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Search Alerts/Recalls
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