WRIGHT MEDICAL TECHNOLOGY INC INTEGRA DEVICE; PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER
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Model Number 60012004 |
Device Problems
Adverse Event Without Identified Device or Use Problem (2993); Appropriate Term/Code Not Available (3191)
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Patient Problems
Damage to Ligament(s) (1952); Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)
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Event Date 02/16/2022 |
Event Type
Injury
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Manufacturer Narrative
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Device will not be returned.If additional information becomes available, it will be provided on a supplemental report.
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Event Description
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It was reported that the patient underwent a revision surgery to remove the hardware and to perform a tendon lengthening of the midfoot; rearfoot or ankle ankle-total ankle arthroplasty; ankle-reconstruction of ankle ligament with graft.
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Event Description
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It was reported that the patient underwent a revision surgery to remove the hardware and to perform a tendon lengthening of the midfoot; rearfoot or ankle ankle-total ankle arthroplasty; ankle-reconstruction of ankle ligament with graft.
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Manufacturer Narrative
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Correction: d1, d4, h6 codes.Please disregard the mfr report as per further received information, the device information confirmed that the reported event is related to an integra product, not a stryker trauma product.
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Search Alerts/Recalls
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