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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC LOCKING BOLT MEASURING DEVICE F/TROCHANTERIC FIXATION NAILS; GAUGE,DEPTH

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WRIGHTS LANE SYNTHES USA PRODUCTS LLC LOCKING BOLT MEASURING DEVICE F/TROCHANTERIC FIXATION NAILS; GAUGE,DEPTH Back to Search Results
Model Number 357.402
Medical Device Problem Code Break (1069)
Health Effect - Clinical Code No Consequences Or Impact To Patient (2199)
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
Investigation summary: investigation flow: visual.Visual inspection: the locking bolt measuring device f/trochanteric fixation nails (p/n: 357.402, lot number: 6957266) was received at us cq.Upon visual inspection, the ball and compression spring components are missing.The shaft tip is also bent backwards.Document/specification review: no design issues or discrepancies were identified.Dimensional inspection: dimensional analysis on the hole for the missing ball and compression spring components could not be performed due to deformation from the staking process that happens during final assembly.Dimensional analysis on the bent shaft tip could not be performed due to device geometry and post-manufacturing damage.Conclusion: the overall complaint was confirmed for the locking bolt measuring device f/trochanteric fixation nails (p/n: 357.402, lot number: 6957266) as the ball and compression spring components are missing and the shaft tip is bent.No definitive root cause could be determined based on the provided information.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: part number: 357.402.Synthes lot number: 6957266.Supplier lot number: n/a.Release to warehouse date: jun 06, 2012.Expiration date: n/a.Manufactured by synthes (b)(4).No ncrs were generated during production.Device history review: review of the device history record showed that there were no issues during the manufacture of this product, and any subcomponents, 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.
 
Event or Problem Description
It was reported on march 24, 2020, a locking bolt measuring device was found broken during reverse logistics audit of the returned device at millstone.There was no patient involvement.This complaint involves one (1) device.This is report 1 of 1 for (b)(4).
 
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Brand Name
LOCKING BOLT MEASURING DEVICE F/TROCHANTERIC FIXATION NAILS
Common Device Name
GAUGE,DEPTH
Manufacturer (Section D)
WRIGHTS LANE SYNTHES USA PRODUCTS LLC
1302 wrights lane east
west chester PA 19380
MDR Report Key9969370
Report Number2939274-2020-01892
Device Sequence Number2437214
Product Code HTJ
UDI-Device Identifier10886982196255
UDI-Public(01)10886982196255
Combination Product (Y/N)N
Initial Reporter StateMA
Initial Reporter CountryUS
PMA/510(K) Number
EXEMPT
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source company representative,health
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 03/24/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model Number357.402
Device Catalogue Number357.402
Device Lot Number6957266
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer03/26/2020
Type of Report(Section G)Initial
Initial Date Received by Manufacturer 03/24/2020
Initial Report FDA Received Date04/16/2020
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
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