Model Number 6000-011-000 |
Device Problems
Incorrect Measurement (1383); Material Twisted/Bent (2981)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 10/07/2022 |
Event Type
malfunction
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Event Description
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Per the customer, the device was bent during a procedure.The procedure was completed successfully without a delay; no adverse consequences or medical intervention was reported.
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Event Description
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Per the customer, the device was bent during a procedure.The procedure was completed successfully without a delay; no adverse consequences or medical intervention was reported.
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Manufacturer Narrative
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Device evaluation: follow-up report submitted to document the device evaluation.
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Search Alerts/Recalls
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