Model Number 1460-000-000 |
Device Problem
Mechanical Jam (2983)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 07/01/2020 |
Event Type
malfunction
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Manufacturer Narrative
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This mdr is part of the fda voluntary malfunction summary reporting program.The device was evaluated in the field and the issue was confirmed; there was an improperly aligned component. the device was repaired and returned.There was no remedial action taken. this device is not labeled for single use.
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Event Description
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This report summarizes 1 malfunction event, where it was reported that the brakes could not be engaged/false engagement of brakes.There was no patient involvement.
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Search Alerts/Recalls
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