SMITH & NEPHEW, INC. PRO METAPH TIB STEM 18MM; PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL
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Catalog Number 71501010 |
Device Problems
Failure to Osseointegrate (1863); Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Pain (1994); Arthralgia (2355); Inadequate Osseointegration (2646)
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Event Date 08/16/2023 |
Event Type
Injury
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Manufacturer Narrative
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Internal complaint number: case-2023-00181613-1 / lgn por ha tib base w/o holes sz 7 lt was reported under: internal complaint number: case-2023-00181401.Report number: 1020279-2023-02364.
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Event Description
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It was reported that, after right tka surgery had been performed on (b)(6) 2022, the patient experienced pain.Furthermore, x-rays showed lucency under the baseplate.This adverse event was treated with revision surgery performed on (b)(6) 2023, in which a lgn por ha tib base w/o holes sz 7 rt,lgn cr high flex xlpe sz 7-8 9mm and a pro metaph tib stem 18mm were exchanged.Patient as far as acknowledged is fit and healthy.
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Event Description
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It was reported that, after right tka surgery had been performed on (b)(6) 2022, the patient experienced pain.Furthermore, x-rays on (b)(6) 2023 showed lucency under the tibial components particularly in the pro metaph tib stem 18mm, this findings would suggest loosening of the protheses.This adverse event was treated with revision surgery performed on (b)(6) 2023, in which a lgn por ha tib base w/o holes sz 7 rt,lgn cr high flex xlpe sz 7-8 9mm and a pro metaph tib stem 18mm were exchanged.Patient as far as acknowledged is fit and healthy.
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Manufacturer Narrative
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Additional information: b6 corrected data corrected data: b3, b5, d1, d4, d10, h4, h6 (health effect - clinical code, medical device problem code).
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Manufacturer Narrative
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H3, h6: the associated devices were returned and evaluated.A visual inspection of the returned stem and insert reveal signs of wear.Both devices have discoloration and scratches on the surface of the devices.The clinical/medical investigation concluded that, based on the reported x-ray findings, prosthetic loosening led to the revision and contributed to the patient¿s pain.The patient impact included the reported pain and bilateral tibial lucency/component loosening with subsequent revision bilaterally.The patient was ¿as far as acknowledged fit and healthy¿, but a post-surgical restorative phase would be anticipated.A review of the production orders did not reveal a manufacturing abnormality that could have caused or contributed to the reported incident.For the stem and the insert, a review of complaint history revealed a similar event for the listed devices over 12 months, but no similar events for the batch based on the historical data, this failure mode will be monitored for future complaints for any necessary corrective actions.For the tibial baseplate, a review of complaint history for the part number over the previous 12 months and for the batch number based on historical data of the device did not reveal similar events for the listed device.A review of the instructions for use documents for knee systems revealed that looseness of components has been identified in possible adverse effects section as a result from trauma, improper implant selection, improper implant positioning, improper fixation, and/or migration of the components.Muscle and fibrous tissue laxity can also contribute to these conditions.A review of the risk management files revealed this failure mode was previously identified.The anticipated risk level is still adequate.A historical review concluded that there are no prior actions related to these products and event.At this time, we have no reason to suspect that the products failed to meet any specifications at the time of manufacture.Factors that could contribute to the reported event include abnormal motion over time, bone degeneration, patient condition and/or traumatic injury.Based on this investigation, the need for corrective action is not indicated.Should 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.Additional information: d7a, d8/d9, h8 corrected data: e1, g2, h6 (health effect - clinical code).
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