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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STRYKER ORTHOPAEDICS-MAHWAH TRIATHLON P/A CR BEADED #2R; PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO

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STRYKER ORTHOPAEDICS-MAHWAH TRIATHLON P/A CR BEADED #2R; PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO Back to Search Results
Catalog Number 5517F202
Device Problems Mechanical Problem (1384); Malposition of Device (2616); Positioning Problem (3009); Appropriate Term/Code Not Available (3191)
Patient Problems Foreign Body In Patient (2687); No Known Impact Or Consequence To Patient (2692)
Event Date 03/07/2016
Event Type  malfunction  
Manufacturer Narrative
An evaluation of the device cannot be performed as the device remained implanted in the patient and was not returned to the manufacturer.Additional information has been requested.Should additional information become available it will be reported in a supplemental report upon completion of the investigation.
 
Event Description
Just after tka surgery, something like 3 beads are found on x-rays.The removal is not planned.
 
Manufacturer Narrative
Reported event: an event regarding disassociation of beads (porous coating) from the triathlon femoral component was reported.The event was confirmed.Method & results: device evaluation and results: not performed as the device was not returned, it remains implanted.Medical records received and evaluation: clinician review of the x-rays provided indicate a mismatch between bone preparation and actual component position has contributed to an overload condition that may easily result in bead shedding from the porous beaded surface layer of the device during final component introduction when the beaded surface rides over the sharp edge of the anterior chamfer cut area.Device history review: dhr review was satisfactory.Complaint history review: chr review confirmed that there were no other similar reported events for the lot.Conclusions: based on clinician review of the x-rays provided indicate a mismatch between bone preparation and actual component position has contributed to an overload condition that may easily result in bead shedding from the porous beaded surface layer of the device during final component introduction when the beaded surface rides over the sharp edge of the anterior chamfer cut area.No further investigation for this event is possible at this time.If devices and / or additional information become available, this investigation will be reopened.Product surveillance will continue to monitor for trends.
 
Event Description
Just after tka surgery, something like 3 beads are found on x-rays.The removal is not planned.
 
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Brand Name
TRIATHLON P/A CR BEADED #2R
Type of Device
PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO
Manufacturer (Section D)
STRYKER ORTHOPAEDICS-MAHWAH
325 corporate drive
mahwah NJ 07430
Manufacturer (Section G)
STRYKER ORTHOPAEDICS-LIMERICK
raheen business park
limerick NA
Manufacturer Contact
sandra spokane
325 corporate drive
mahwah, NJ 07430
2018315000
MDR Report Key5534478
MDR Text Key41482322
Report Number0002249697-2016-01011
Device Sequence Number1
Product Code MBH
Combination Product (y/n)N
PMA/PMN Number
K141056
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type health professional,other
Reporter Occupation Physician
Type of Report Initial,Followup
Report Date 03/07/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/30/2016
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Expiration Date12/31/2020
Device Catalogue Number5517F202
Device Lot NumberAMB3M1
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Date Manufacturer Received06/16/2016
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured12/20/2015
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age64 YR
Patient Weight55
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