| Model Number |
ZCT450 |
| Medical Device Problem Code |
Adverse Event Without Identified Device or Use Problem (2993)
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| Health Effect - Clinical Codes |
Blurred Vision (2137); No Code Available (3191)
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| Date of Event |
02/20/2017
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Type of Reportable Event
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Serious Injury
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Additional Manufacturer Narrative
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(b)(4).All pertinent information available to the manufacturer has been submitted.
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Event or Problem Description
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It was reported that a model zxt375 29.5 diopter intraocular lens (iol) was explanted from a female patient's right eye due to complications of iol, blurry vision.The lens was replaced with the same model, a smaller, 29.0 diopter lens.No further information was provided.
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Additional Manufacturer Narrative
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Correction - account reported they initially provided an incorrect serial number and model for the reported event for the right eye.A corrected model and serial number was provided and the following fields were updated accordingly: it was reported that a model zct450 29.0 diopter intraocular lens (iol) was explanted from a female patient's right eye due to complications of the intraocular lens (iol), blurry vision.The lens was replaced with a zxt375 29.0 diopter lens.No patient injury was reported.Additionally it was reported that the patient also underwent explant of the lens implanted in her left eye.A separate mdr will be filed for the lens from the left eye.Expiration date 2/18/2021.Model zct450.Catalog number zct450u290.Serial (b)(4).Implant date (b)(6) 2016.Manufacturing date 02/08/2016.All pertinent information available to abbott medical optics has been submitted.
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Additional Manufacturer Narrative
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Device evaluation: the intraocular lens (iol) was not returned to the manufacturing site.Therefore, product testing could not be performed and the customer¿s reported complaint could not be verified.Manufacturing records review: the manufacturing records for the intraocular lens were reviewed.The product was manufactured and released according to specification.A search on complaints revealed no similar complaints have been received for this production order.Labeling review: the directions for use (dfu) was reviewed.The dfu adequately provides instructions and precautions along with warnings for the proper use and handling of the device.As a result of the investigation there is no indication of a product quality deficiency and the reported issue could not be verified.All pertinent information available to abbott medical optics has been submitted.
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Search Alerts/Recalls
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