A2 - age/date of birth: the exact date of birth is unknown, but the age 81 was provided.Section a4 and a5: per regulation eu 2016/679 (general data protection regulation), patient identifiers were not collected or recorded and therefore are not available.D6a - implant date: not applicable, as the lens was not implanted.D6b - explant date: not applicable, as the lens was not implanted.E1: initial reporter first name: unknown, as information was asked but it was not provided.E1: email address: unknown/not provided, as information was asked but it was not provided.E1 - telephone number: (b)(6).H3 - other (81): the intraocular lens (iol) was not returned for evaluation.Therefore, a failure analysis of the complaint device could not 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 and possible product return and evaluation, if there is any further relevant information a supplemental medwatch will be filed.All pertinent information available to johnson and johnson surgical vision, inc.Has been submitted.
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