STRYKER GMBH TIBIAL COMP,SINGLECOATED US VERS, X-LARGE; PROSTHESIS, KNEE, FEMOROTIBIAL, UNICOMPARTMENTAL, SEMI-CONSTRAINED, METAL/POLYME
|
Back to Search Results |
|
Catalog Number 400264 |
Device Problem
Device Operates Differently Than Expected (2913)
|
Patient Problems
Cyst(s) (1800); Pain (1994)
|
Event Date 05/26/2011 |
Event Type
Injury
|
Manufacturer Narrative
|
The reported device was manufactured and distributed by (b)(4)., (b)(4) and implanted prior to (b)(4) purchase of certain assets of (b)(4) on august 1, 2014.Stryker became legal manufacturer of this product on april 1, 2015 and has taken the responsibility for medical device reporting.Device remains implanted.Additional information was requested and if received will be provided on a supplemental report.
|
|
Event Description
|
Patient was having pain on medial malleolus side of her ankle.Imaging revealed a cyst in the medial malleous.Surgery was performed to remove cyst.Medication was prescribed.During the surgery, the surgeon noted no observation for all star components.Two weeks after the surgery, the patient reported of having spontaneous pain about the medial malleolus on the posterior side.
|
|
Manufacturer Narrative
|
All implants were classified as primary products during investigation.No deviations were found during review of the manufacturing and inspection documents (dhr).The implants were documented as faultless prior to distribution.The study records included that a bone cyst was detected after ~9 years in the medial malleolus.After approx.One year tenderness over the tibial tendon behind the medial malleolus was detected; the study records does not include information that reports pain in the medial malleolus after two weeks from the revision surgery; therefore this part of the event description cannot be confirmed.Because no further information about the tenderness was included in the study records the root cause could not be determined.Cysts were already evaluated by a hcp in the statement ¿clinical results of the star ankle prosthesis, page 70, 71¿: ¿cyst formation (bone resorption) (0 ¿ 16 %) [1, 6, 9, 10, 12, 13, 15, 17, 20, 24, 27, 28, 30].Spontaneous bone resorption and cyst formation represents a significant problem in ankle arthroplasty.The symptoms may be mild and will not require specific surgical measures, but in many cases revision surgery with bone grafting may be required.In advanced cases cyst formation may cause a collapse of the arthroplasty requiring implant removal and ankle fusion.¿ additionally cysts were evaluated by a product expert from the development department: ¿this is a known complication and risk in the scientific literature.The exact source is unknown.Researchers believe that it is due to poly wear debris and/or fluid hydraulic pressure in the joint.¿ nevertheless, osteolysis and/or other periprosthetic bone loss (like cysts); furthermore pain, are adverse effects and may require medical or surgical intervention (therefore listed in the ifu).Conclusion: based on the evaluation a manufacturing issue was not found but a correlation between the implant and the cyst cannot be excluded.The case represents a recurring issue for the sliding core and tibial component and will be monitored and evaluated according to pms trending procedure (b)(4).No non-conformity was detected.Device was revised but not returned for investigation.
|
|
Event Description
|
Patient was having pain on medial malleolus side of her ankle.Imaging revealed a cyst in the medial malleous.Surgery was performed to remove cyst.Medication was prescribed.During the surgery, the surgeon noted no observation for all star components.2 weeks after the surgery, the patient reported of having spontaneous pain about the medial malleolus on the posterior side.
|
|
Search Alerts/Recalls
|
|
|