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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER EDGEPLUS VALVED ENTRY SYSTEM; CANNULA, TROCAR, OPHTHALMIC

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ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER EDGEPLUS VALVED ENTRY SYSTEM; CANNULA, TROCAR, OPHTHALMIC Back to Search Results
Catalog Number 8065751586
Medical Device Problem Code Material Twisted/Bent (2981)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 11/26/2024
Type of Reportable Event Malfunction
Event or Problem Description
A physician reported that an ophthalmic trocar tip was found bent during surgery.The surgery was completed after replacing a product with a new one.Surgery details were not provided, no patient impact was reported.
 
Additional Manufacturer Narrative
Investigation including root cause analysis is in progress.A supplemental mdr will be filed as necessary in accordance with 21 cfr 803.56 when additional reportable information becomes available.The manufacturer internal reference number is: (b)(4).
 
Additional Manufacturer Narrative
Additional information was provided in sections d.9, h.3, h.6 and h.11.Corrected information provided in section h.6.A review of the device history record traceable to the reported lot number, indicates that the reported product was processed and released according to the reported product¿s acceptance criteria.The exact root cause could not be determined from the investigation performed.The returned sample is visually non-conforming with the tip of the knife bent; therefore, a bent knife prior to patient contact was confirmed; however, how and when the tip of the knife became bent could not be determined.The exact root cause for the bent knife sample is unknown, therefore specific action with regards to this complaint cannot be taken.All trocar blades are (b)(4) inspected.Any nonconformance, such as the damaged tip exhibited on the returned opened sample is removed from the lot and scrapped.Complaints are reviewed and monitored at regular intervals for any significant adverse trends.No adverse trends have been observed associated with the reported product and event.No further actions are required.The manufacturer internal reference number is: (b)(4).
 
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Brand Name
EDGEPLUS VALVED ENTRY SYSTEM
Common Device Name
CANNULA, TROCAR, OPHTHALMIC
Manufacturer (Section D)
ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER
15800 alton parkway
irvine CA 92618
Manufacturer (Section G)
ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER
15800 alton parkway
irvine CA 92618
Manufacturer Contact
jonathan schlech
6201 south freeway
mail stop ab2-6
fort worth, TX 76134
8007579780
MDR Report Key21100773
Report Number2028159-2025-00032
Device Sequence Number8935295
Product Code NGY
UDI-Device Identifier00380657515868
UDI-Public(01)00380657515868(17)250430(11)230504(10)15L445
Combination Product (Y/N)N
Initial Reporter CountryJA
PMA/510(K) Number
EXEMPT
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional,Company Representative
Initial Reporter Occupation Physician
Type of Report Initial,Followup
Report Date (Section B) 04/09/2025
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 Expiration Date04/30/2025
Device Catalogue Number8065751586
Device Lot Number15L445
Was Device Available for Evaluation? Device Returned to Manufacturer
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Initial
Initial Date Received by Manufacturer 12/11/2024
Supplement Date Received by Manufacturer03/13/2025
Initial Report FDA Received Date01/08/2025
Supplement Report FDA Received Date04/09/2025
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured05/04/2023
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Concomitant Medical Products
and Therapy/Usage Dates
CONSTELLATION VISION SYSTEM.
Patient SexUnknown
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