Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Dry Eye(s) (1814); Intraocular Pressure Increased (1937); Eye Pain (4467)
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Event Type
Injury
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Manufacturer Narrative
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Product code: unk; claim#: (b)(4).
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Event Description
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(b)(6) complaint: the reporter indicated that the surgeon implanted an implantable collamer lens (icl) into the patient's eye.The patient reports elevated iop, and painful dry eye.Attempts to obtain additional information have not been successful.
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Manufacturer Narrative
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On (b)(6) 2020, it was determined that this case is a duplicate of mfr report# 2023826-2019-00729.Please disregard the current report.Claim# (b)(4).
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Search Alerts/Recalls
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