Additional narrative: reporter is a j&j employee.A device history record (dhr) review was conducted: visual inspection: the complaint device depth gauge for lckng scrs to 100 (product code: 03.010.072, lot number: l832726) was returned to cq west chester for investigation.During visual inspection, the depth gauge needle was bent and deformed.The gauge was missing the body cover and the dowel pin on the slider.Document /specification review: based on the date of manufacture, the current and manufactured version of the drawings were reviewed.Locking screw measuring device for 188mm sleeve, 03_010_072, rev h (current) and rev f(manufactured) body locking screw measuring device, 03_010_071_1 rev d (current) and rev c (manufactured) slider assembly, 03_010_072_2, rev h (current) and rev f(manufactured) dowel pin, es0003-19 rev f (current and manufactured) hook slider assembly, 03_010_072_2_2 rev d (current and manufactured) se_022863 rev af dimensional inspection: according to 03_010_072_2_2 rev d, diameter: 1.1 mm ± 0.1 mm (specified dimension) diameter: 1.06 mm (measured dimension, conforming) conclusion: the depth gauge needle was bent at the hook, missing the cover and the dowel pin.A definitive root cause was not determined during investigation.There was no indication that a design or manufacturing issue contributed to the complaint.No design issues were observed during the document/specification review.Based on the investigation findings, it has been determined that no corrective and/or preventative action is proposed.Additional monitoring for any potential safety signals will be conducted through complaint trending and other post-market safety surveillance activities.Device history lot - no ncrs were generated during production.Device history review - 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.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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