| Model Number |
DCB00 |
| Medical Device Problem Code |
Break (1069)
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| Health Effect - Clinical Code |
No Clinical Signs, Symptoms or Conditions (4582)
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| Date of Event |
10/24/2025
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Type of Reportable Event
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Malfunction
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Additional Manufacturer Narrative
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Section a2, a3, a4, and a5: per regulation eu 2016/679 (general data protection regulation), patient identifiers were not collected or recorded and therefore are not available.Section d6b - explant date: n/a - lens remains implanted; therefore, not explanted.Section e1 - telephone number: (b)(6) section h3: the device was not returned for evaluation; therefore, a failure analysis of the complaint device cannot be completed.A review of records including device history and complaint trending will be performed.Upon completion of this review, 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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Event or Problem Description
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It was reported that post implantation of the preloaded, monofocal, intraocular lens (iol) the surgeon noted a defect along the edge of the iol which was only visible under the microscope.No further information was provided.
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Additional Manufacturer Narrative
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Additional information: section d9 - device available for evaluation? yes section h3 - device evaluated by manufacturer? yes device evaluation: no suspect product was received; however, a photograph provided by the customer was evaluated.The picture showed a pseudophakic eye implanted with a tecnis monofocal lens preloaded in the simplicity delivery system model dcb00.A crack like mark was observed in the lens periphery between 12:30 and 1:30 per the picture orientation.The location of the mark was not expected to impact the patient visual function, in the event the lens remains implanted; however, the definitive clinical impact or the potential root cause of the reported incident could not be determined by the picture assessment.Conclusion: as a result of the investigation, there is no indication of a product quality deficiency.All pertinent information available to johnson and johnson surgical vision, inc.Has been submitted.
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Search Alerts/Recalls
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