On july 11, 2022, a notification was received indicating that a patient, listed on the shoulder arthroplasty registry, is experiencing worsening pain.An x-ray shows a dislodged glenoid component.Surgeon has scheduled the patient for a revision surgery to an rsa on (b)(6) 2022.Original surgery took place on (b)(6) 2020.Additional information received on 7/12/2022: during surgery on (b)(6) 2020, a total of 4 arthrex devices were implanted.An ar-9301-03 eclipse cage screw large, lot number 19.00501, an ar-9301-43cpc eclipse trunion, lot number 18-01245, an ar-9343-16 eclipse humeral head, lot number 1917001, and an ar-9106-01 univers vaultlock glenoid.As of now, nothing has shown to be broken inside the patient but there's a dislodgment of glenoid prosthesis.Additional information received on 7/25/2022: according to facility representative, patient experienced cardiac events during the pre-op area and revision surgery did not take place.At this time, it is unknown if patient will undergo revision surgery.Additional information received on 12/30/2022: the revision surgery that was to take place on (b)(6) 2022, was cancelled due to cardiac co-morbidities.No further information has been provided.
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