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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Alcon Research, LLC - Huntington MONARCH III IOL Delivery System, Cartridge D; Folders and Injectors, Intraocular Lens (IOL)

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Alcon Research, LLC - Huntington MONARCH III IOL Delivery System, Cartridge D; Folders and Injectors, Intraocular Lens (IOL) Back to Search Results
Catalog Number 8065977763
Medical Device Problem Code Scratched Material (3020)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/04/2026
Type of Reportable Event Malfunction
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Brand Name
MONARCH III IOL Delivery System, Cartridge D
Common Device Name
Folders and Injectors, Intraocular Lens (IOL)
Manufacturer (Section D)
Alcon Research, LLC - Huntington
246 kyle lane
huntington WV 25702
Manufacturer (Section G)
Alcon Research, LLC - Huntington
246 kyle lane
huntington WV 25702
Manufacturer Contact
jonathan schlech
6201 south freeway
mail stop ab2-6
fort worth, TX 76134
+1(800)757-9780
MDR Report Key50559340
Report Number1119421-2026-01799
Device Sequence Number21314230
Product Code MSS
UDI-Device Identifier00380659777639
Combination Product (Y/N)N
Initial Reporter StateTX
Initial Reporter CountryUS
PMA/510(K) Number
K063155
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Company Representative
Initial Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date (Section B) 09/02/2026
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 Catalogue Number8065977763
Device Lot Number16210628
Was Device Available for Evaluation? Yes
Date Returned to Manufacturer09/01/2026
Is the Reporter a Health Professional? No
Initial Date Received by Manufacturer 08/05/2026
Initial Report FDA Received Date09/02/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured02/23/2026
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 Age78 YR
Patient SexFemale
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