Product evaluation: the product was not returned.Product history records were reviewed and the documentation indicated the product met release criteria.The product investigation could not identify a root cause.Information was provided that the lens was implanted on (b)(6) 2017.After a day of treatment on (b)(6) 2017, the patient was more comfortable.On (b)(6) 2017, the patient's postoperative adverse symptoms disappeared.There have been no other complaints reported in the lot number.The manufacturer internal reference number is: (b)(4).
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A health authority reported tearing, congestion, redness, pain and corneal edema in an eye following an intraocular lens (iol) implant procedure.The patient was treated with medication.Symptoms recovered.The lens remains implanted.
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