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.D2b additional device product codes: gxl and hwe.H3, h4, h6: part # 05.000.008.Synthes lot # 008084.Supplier lot #: 008084.Release to warehouse date: 13 dec 2021.Supplier: triangle manufacturing.No ncr's generated during production.Review of the device history record(s) showed that there were no issues during the manufacture of this product, and any sub-components, which would contribute to this complaint condition.Service and repair evaluation: the customer reported that no speed works in 05.000.008, hand piece for battery powered driver.The repair technician reported that brown residue was present on motor and barriers.Damaged component is the reason for repair.The cause of the issue is unknown.The following parts were replaced: circuit board, set screw, housing barrier, shrink tubing and all other applicable components.The item was repaired per the inspection sheet and will be returned to the customer upon completion of the service and repair process.The evaluation was confirmed.The device was deemed serviceable and will be returned to the customer, no design or manufacturing issues were identified therefore it has been determined that no corrective and/or preventative action is proposed.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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