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DEPUY SYNTHES PRODUCTS LLC MOTOR ASSEMBLY, XMAX; DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE
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| Catalog Number |
XMAX |
| Medical Device Problem Code |
Premature Separation (4045)
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| Health Effect - Clinical Code |
No Clinical Signs, Symptoms or Conditions (4582)
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| Date of Event |
01/01/2025
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Type of Reportable Event
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Malfunction
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Event or Problem Description
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It was reported that the motor device kept releasing the cutter device during surgery.There were no reports of delays to a surgical procedure.During in-house engineering evaluation, it was determined that the device hose was damaged, was leaking a liquid, was missing components and had insufficient/low power.The device also failed pretests for visual assessment, hose assessment, muffler tube assessment, rotational speed assessment and oil leak assessment.There were no reports of injuries, medical intervention or prolonged hospitalization.The date of event was unknown but was known to have occurred in 2025.All available information has been disclosed.
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Additional 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.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.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.H11 additional narrative: the actual device was returned for evaluation.The device was evaluated and it was determined that the reported condition was not confirmed.Therefore, the assignable root cause was not determined.However, during evaluation, it was determined that the device hose was damaged, was leaking a liquid, was missing components and had insufficient/low power.The device also failed pretests for visual assessment, hose assessment, muffler tube assessment, rotational speed assessment and oil leak assessment.The assignable root cause was traced to user error.
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