It was reported through the surgical outcome system that a patient may have had an issue as a result of surgery involving arthrex implants.Upon further investigation it was discovered that a patient had a (b)(6) 2019 reverse shoulder replacement procedure.After the nerve block had worn off, approximately 24 hours post surgery the patient was experiencing numbness in the surgical arm's palm, half of ring finger and the pinkie finger.The patient was diagnosed with ulnar nerve palsy and told it may take a year to resolve.Patient consulted with a neurologist, who said nothing could be done.The ulnar nerve was damaged.No second surgery has been performed.The following are the arthrex products that were implanted (b)(6) 2019: ar-9560 28-4, lot: 6094, ar-9561-25p, lot: 5685, ar-9502f-39rcpc, lot: 19.00275, ar-9501-105, lot: 18.0037, ar-9564-2839-lat, lot: 18.02027, ar-9562-28nl,lot: 2018005880, ar-9503m-06, 19.00667, ar-9563-28, lot: 2019001687, ar-9563-24, lot: 19.02242, ar-9562-28nl, lot: 2018005880.
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