SMITH & NEPHEW, INC. UNKN JOURNEY UNI KNEE FEM COMP; PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER
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Catalog Number UNKN01200322 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Pain (1994); Loss of Range of Motion (2032)
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Event Date 02/22/2022 |
Event Type
Injury
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Event Description
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On the literature review " combined procedures with unicompartmental knee arthroplasty: high risk of stiffness but promising concept in selected indications", it was reported that, after undergoing a navio-assisted uka procedure using journey ii uni system, one (1) patient experienced pain and stiffness.These event was treated with a revision surgery to tka.No further information is available.All available information has been disclosed.If additional information should become available, a supplemental report will be submitted accordingly.
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Manufacturer Narrative
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Smith & nephew is submitting this report pursuant to the provisions of 21 c.F.R.Part 803.This report may be based upon information which smith & nephew has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, smith & nephew, or its employees, that the report constitutes an admission that the device, smith & nephew or its employees caused or contributed to the potential event described in this report.Derreveaux, v, et al.(2022).Combined procedures with unicompartmental knee arthroplasty: high risk of stiffness but promising concept in selected indications.Sicot-j (vol.8, no 4).Doi: 10.1051/sicotj/2022002.(b)(4).
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Manufacturer Narrative
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H3, h6: the device was not returned for evaluation and the reported event could not be confirmed.The clinical/medical investigation concluded that, as of the date of this medical investigation, the requested clinical documentation has not been received.Reportedly, no further information is available.The author has provided radiological assessment of the imaging within the text; therefore, further analysis is not warranted.Without the requested medical documentation, definitive clinical factors which could have contributed to the reported event could not be concluded.The patient outcome beyond that which was reported could not be determined.No further medical assessment can be rendered at this time.At this time, we have no reason to suspect that the product failed to meet any product specifications at the time of manufacture.Possible causes could include but not limited to traumatic injury, joint tightness, patient reaction, postoperative care, alignment or fit/size of device used.The contribution of the device to the reported event could not be corroborated.Based on this investigation, the need for corrective action is not indicated.Without the return of the actual product involved, our investigation could not proceed.Should the device or additional information be received, the complaint will be reopened.No further investigation is warranted for this complaint; however, we will continue to monitor for future complaints and investigate as necessary.We consider this investigation closed.Internal complaint reference number: (b)(4).
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