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Catalog Number 530.710 |
Device Problems
Mechanical Jam (2983); Intermittent Loss of Power (4016)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/01/2024 |
Event Type
malfunction
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Event Description
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It was reported by switzerland that during service and evaluation, it was determined that the battery oscillator device operated intermittently due to a damaged controller.It was further determined that the device failed pretest for check function of device and check oscillation frequency with frequency meter.It was noted in the service order that during an unspecified surgical procedure, it was discovered that the device got stuck.It was reported that there were no delays in the surgical procedure as a spare device was used to complete the surgery.There was patient involvement reported.There were no reports of injuries, medical intervention, or prolonged hospitalization.The exact date of the event was unknown.However, it was reported that the event occurred in january 2024.All available information has been disclosed.If additional information should become available, a supplemental medwatch report will be submitted accordingly.
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Manufacturer Narrative
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This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information which has not been investigated or verified prior to the required reporting date.This report does not reflect a conclusion by depuy synthes, or its employees that the report constitutes an admission that the product, depuy synthes, or its employees caused or contributed to the potential event described in this report.Device was used for treatment, not diagnosis.If information is obtained that was not available for this medwatch, a supplemental medwatch report will be filed as appropriate.H10 additional narrative: service review: a review of the service history record indicates that the device has been serviced within the last year for a service condition that is not relevant to the current reported condition.Device evaluation: the actual device was returned for evaluation.During repair, an evaluation was performed, and it was determined that the reported condition of the device being stuck was not confirmed.Therefore, an assignable root cause was not determined.However, the device having intermittent operation, identified during service and evaluation was confirmed.The assignable root cause was determined to be due to component failure from normal wear.Udi:(b)(4).
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Search Alerts/Recalls
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