SMITH & NEPHEW, INC. GII NP FIN-STEM PUNCH S3-4; PROST, KNEE, FEMTIB, SEMI-CNSTRND, CMNTD, MET/POLY
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Model Number 71449993 |
Device Problems
Fracture (1260); Material Deformation (2976)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 08/02/2022 |
Event Type
malfunction
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Manufacturer Narrative
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Internal complaint reference: (b)(4).
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Event Description
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It was reported that, during a tka surgery, a gii np fin-stem punch s3-4 was chipping distally and intraoperative.There was no evidence of broken material in the patient's joint on post-operative x-ray check.The procedure was completed, with no delay, using the same device.Patient was not harmed as consequence of this problem.
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Manufacturer Narrative
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Additional information: expiration date) and h4, corrected data: d4 (lot number).
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Manufacturer Narrative
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H3, h6: the associated device was returned and evaluated.A visual inspection of the returned device confirms the tip of the device is severely damaged.The tip has multiple gouges, burrs and there are pieces of metal chipped away from the device.The device shows signs of extreme wear and use.A review of complaint history revealed similar events for the listed device over the previous 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.A review of the manufacturing records did not reveal a manufacturing abnormality that could have caused or contributed to the reported incident.At this time, we do not have reason to suspect that the product failed to meet any product specifications at the time of manufacture.A review of the risk management file revealed this failure mode was previously identified.The anticipated risk level is still adequate.Assessment of historical escalated cases concluded that there are no prior actions related to this device and failure mode.As the device broke and it can no longer fit its purpose, the contribution of the device to the reported event could be corroborated.This device is a reusable instrument that can be exposed to numerous surgeries.Damage from prolonged use, misuse or rough handling are likely potential factors that could contribute to the reported event.We recommend that all reusable instruments be routinely inspected for wear and damage and replaced as necessary.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 future complaints and investigate as necessary.We consider this investigation closed.Internal complaint reference number: (b)(4).
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