Patient weight and ethnicity: unknown; requested but not provided.Date of event: unknown; requested but not provided.The best estimate date is on (b)(6).2022.The device was not returned for evaluation as it was discarded; therefore, a failure analysis of the complaint device cannot be completed.A review of the device history record, complaint trending, and risk documentation for this device will be performed.Upon completion of the review, if there is any further relevant information a supplemental medwatch will be filed.Multiple attempts have been made to obtain additional information regarding the event; however, to date, no response has been received.All pertinent information available to johnson & johnson surgical vision, inc.Has been submitted.
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It was reported that the intraocular lens (iol) was explanted in a secondary procedure due to the patient being unsatisfied with near vision.Another johnson & johnson iol (different model, zkb, different diopter, 19.0).The patient is fine and doing well.The lens is not available for return.No further information was provided.
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