STERILE FIELD POST AND ARM, FEMUR ELEVATOR 11502R

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2016-08-31 for STERILE FIELD POST AND ARM, FEMUR ELEVATOR 11502R manufactured by Integra Lifesciences Corporation Oh/usa.

Event Text Entries

[53565642] To date the device involved in the reported incident has not been received for evaluation. An investigation has been initiated based on the reported information.
Patient Sequence No: 1, Text Type: N, H10


[53565643] Customer initially reports the unit slips and will not hold tension. (b)(6) 2016 customer reports no harm done, no damage, no further information available.
Patient Sequence No: 1, Text Type: D, B5


[58377190] 10/4/16 integra investigation completed. Manufacture date unknown. Method: failure analysis, device history evaluation. Results: device history evaluation - device history record reviewed for these product ids under lot codes 154 and 159 respectively show no abnormalities related to reported incident found. This device passed all required inspection points with no associated mrr? S, variances or rework. No previous service history is on file. These parts have not been in for service as these parts were the replacements from previous repairs. Conclusion: upon further investigation into the customer? S complaint, engineering noticed the s. F. Clamp subassembly was not functioning properly as designed. The s. F clamp subassembly primarily comprises of two clamps, a. 50 serrated clamp and a. 75 serrated clamp which lock together when the handle is placed in the locked position. In the locked position, the starburst teeth do fully engage with no visible gaps present yet the handle does not align parallel to the field post. A dysfunctional, likely bent, internal component within the. 50 serrated clamp assembly is likely the main cause for the s. F clamp subassembly not properly tightening onto the field post. The cam body is supposed to fully sit on the bushing at all times in both locked and unlocked positions. The handle should always remain parallel to the field post when fully rotated to either end. The handle should only have the ability to rotate between 0? And 180? , even with the application of force. It is highly likely overexertion of force to lock the clamp is a major contributor and possible root cause for this failure, based on the indications on the 4047011 cam body and 10480 handle..
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2125289-2016-00007
MDR Report Key5917133
Report SourceUSER FACILITY
Date Received2016-08-31
Date of Report2016-08-12
Date Mfgr Received2016-10-04
Date Added to Maude2016-08-31
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactUSER SANDRA LEE
Manufacturer Street311 ENTERPRISE DRIVE
Manufacturer CityPLAINSBORO NJ 08536
Manufacturer CountryUS
Manufacturer Postal08536
Manufacturer Phone6099362393
Manufacturer G1INTEGRA LIFESCIENCES CORPORATION OH/USA
Manufacturer Street4900 CHARLEMAR DRIVE
Manufacturer CityCINCINNATI OH 45227
Manufacturer CountryUS
Manufacturer Postal Code45227
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTERILE FIELD POST AND ARM, FEMUR ELEVATOR
Generic NameSURGICAL RETRACTOR
Product CodeFFO
Date Received2016-08-31
Returned To Mfg2016-08-25
Catalog Number11502R
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerINTEGRA LIFESCIENCES CORPORATION OH/USA
Manufacturer Address4900 CHARLEMAR DRIVE 4900 CHARLEMAR DRIVE CINCINNATI OH 45227 US 45227


Patients

Patient NumberTreatmentOutcomeDate
10 2016-08-31

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