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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: AMO PUERTO RICO MFG. INC. TECNIS SIMPLICITY; INTRAOCULAR LENS

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AMO PUERTO RICO MFG. INC. TECNIS SIMPLICITY; INTRAOCULAR LENS Back to Search Results
Model Number DCB00
Medical Device Problem Code Break (1069)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 10/24/2025
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
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.
 
Event or Problem Description
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.
 
Additional Manufacturer Narrative
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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Brand Name
TECNIS SIMPLICITY
Common Device Name
INTRAOCULAR LENS
Manufacturer (Section D)
AMO PUERTO RICO MFG. INC.
road 402 north, anasco ind. pk
anasco PR 00610
Manufacturer Contact
somyata negpal
31 technology street
irvine, CA 92618
7142478552
MDR Report Key23609334
Report Number3012236936-2025-000288
Device Sequence Number9444969
Product Code HQL
UDI-Device Identifier05050474636149
UDI-Public(01)05050474636149(17)280804
Combination Product (Y/N)N
Initial Reporter CountryUK
PMA/510(K) Number
P980040
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2025
Serviced by Third Party (Y/N)Unknown
Reporter Type Manufacturer
Report Source Foreign,Health Professional,User Facility
Initial Reporter Occupation Physician
Type of Report Initial,Followup
Report Date (Section B) 01/06/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model NumberDCB00
Device Catalogue NumberDCB0000230
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 10/27/2025
Supplement Date Received by Manufacturer12/12/2025
Initial Report FDA Received Date11/20/2025
Supplement Report FDA Received Date01/06/2026
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured08/04/2025
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Patient SexUnknown
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