WRIGHTS LANE SYNTHES USA PRODUCTS LLC GRAPHIC CASE FOR MODULAR HAND SYSTEM; TRAY,SURGICAL INSTRUMENT
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Model Number 690.377 |
Device Problems
Crack (1135); Device-Device Incompatibility (2919)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Type
malfunction
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Event Description
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Device report from synthes reports an event in the usa as follows: it was reported that on an unknown date the instrument unable to sterilize or assemble.It was chipping and cracking, unable to use.Need replacement as soon as possible.No patients involvement is there.This complaint involves (1) device unk - cases/trays/modules.This is report 1 of 1 for complaint (b)(4).
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Manufacturer Narrative
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Product complaint # (b)(4).This report is for an unk - cases/trays/modules/unknown lot.Part and lot numbers are unknown; udi number is unknown.Complainant part is expected to be returned for manufacturer review/investigation but has yet to be received.Reporter is a j&j sales representative.Without a lot number the device history records review could not be completed.Product was not returned.Based on the information available, it has been determined that no corrective and/or preventative action is proposed.This complaint will be accounted for and monitored via post market surveillance activities.If additional information is made available, the investigation will be updated as applicable.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Manufacturer Narrative
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Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.If the information is unknown, not available or does not apply, the section/field of the form is left blank.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Event Description
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This report is for a graphic case for modular hand system.
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Search Alerts/Recalls
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