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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - VEPTR IMPLANTS: PARALLEL CONNECTOR; PROSTHESIS, RIB REPLACEMENT
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WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - VEPTR IMPLANTS: PARALLEL CONNECTOR; PROSTHESIS, RIB REPLACEMENT Back to Search Results
Catalog Number 04.641.056
Device Problem Device Slipped (1584)
Patient Problem No Code Available (3191)
Event Type  Injury  
Manufacturer Narrative
This report is for an unknown veptr implants: parallel connector/ unknown lot.Part and lot number are unknown; udi number is unknown.Complainant part is not expected to be returned for manufacturer review/ investigation.Reporter is a synthes employee.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.(b)(4).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 Description
It was reported that on (b)(6) 2019 that the patient underwent the removal of an adaptor.When the surgeon removed the proximal distal rod articulate, where the connection is made that is supposed to be rigid, the parallel connector was not holding the rod.Patient status and outcome were unknown.Concomitant device reported: unknown rod (part # unknown, lot # unknown, quantity# 2).This report is for one (1) unk - veptr implants: parallel connector.This is report 1 of 1 for (b)(4).
 
Event Description
Concomitant devices: titanium (ti) distal extension size 6/500mm radius (part: 04.641.076, lot: 9953122, quantity: 1), ti distraction lock (part: 497.125, lot: h688156, quantity: 1).
 
Manufacturer Narrative
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.H10 additional narrative: b5 d1, d4, d11.H3, h6: the device was received, the investigation is in progress, no conclusion could be drawn at the time of filing this report.H11 corrected data: d10, h3.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.
 
Manufacturer Narrative
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.H10 additional narrative: g1: physical manufacturer.H3, h6: a product investigation was conducted.Visual inspection: the unk- vertr implants: parallel connector (p/n:04.641.056, lot #:7775087) was returned and received assembled with titanium distal extension size 6/500mm radius (p/n: 04.641.076) and titanium distraction lock (497.125) at us cq.Upon visual inspection, it was observed that the proximal side of the rod where the parallel connector was supposed to be right with ti distal extension when connected with the ti distraction lock was broken causing the parallel connector articulate.There were nicks and scratches on the device which could be due to explantation and has no impact on the functionality of the device.No other issues were identified with the returned components of the device.Dimensional inspection: no dimensional inspection can be performed due to post-manufacturing damage.Furthermore, the complaint relevant dimensions cannot be checked for dimensional accuracy, because of the design of the device.Document/specification review: based on the date of manufacture the following drawings, reflecting the current and manufactured revision were reviewed investigation conclusion: the complaint condition is confirmed for the unk- vertr implants: parallel connector (p/n:04.641.056, lot #:7775087) is broken, which could have contributed to the complaint condition.There is no indication that a design or manufacturing issue has caused the breakage and hence the root cause cannot be determined.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.H3, h4, h6: a device history record (dhr) review was conducted: part number: 04.641.056; lot number: 7775087; per jde, manufactured date: 09/09/14; a manufacturing related potential cause was not suspected, therefore no manufacturing record evaluation is required.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.
 
Manufacturer Narrative
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.H10 additional narrative: h11 corrected information: d1, d2, d3, d4, g5-510k: this report is for an unknown veptr implants: parallel connector/unknown lot.Part and lot number are unknown; udi number is unknown.G1: physical manufacturer is unknown.H3, h6: customer quality investigation: the compliant device was not received for investigation.The following investigation is based on the image(s) provided.The x-ray was reviewed, and the complaint condition could not be confirmed for not holding the rod/ loose by reviewing the x-ray provided.Since the device was not returned, a dimensional inspection and a functional test were not able to be performed.A definitive assignable root cause could not be determined based on the provided information.Conclusion: during the investigation, no product design issues or discrepancies were observed (based on the images) that may have contributed to the complaint condition.Additional monitoring for any potential safety signals will be conducted through complaint trending and other post-market safety surveillance activities.Based on the investigation findings, 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.
 
Event Description
This is report 1 of 2 for (b)(4).
 
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Brand Name
UNK - VEPTR IMPLANTS: PARALLEL CONNECTOR
Type of Device
PROSTHESIS, RIB REPLACEMENT
Manufacturer (Section D)
WRIGHTS LANE SYNTHES USA PRODUCTS LLC
1302 wrights lane east
west chester PA 19380
MDR Report Key9437566
MDR Text Key170046532
Report Number2939274-2019-62558
Device Sequence Number1
Product Code MDI
Combination Product (y/n)N
PMA/PMN Number
K142587
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative
Type of Report Initial,Followup,Followup,Followup
Report Date 11/18/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/09/2019
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Catalogue Number04.641.056
Device Lot Number7775087
Was Device Available for Evaluation? No
Date Returned to Manufacturer12/10/2019
Date Manufacturer Received01/16/2020
Patient Sequence Number1
Treatment
TI DISTAL EXTENSION SIZE 6/500MM RADIUS; TI DISTRACTION LOCK; UNK - RODS; UNK - RODS
Patient Outcome(s) Required Intervention;
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