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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Alcon Research, LLC - Huntington AcrySof IQ Singlepiece IOL with ULTRASERT Delivery System; Lens, Guide, Intraocular

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Alcon Research, LLC - Huntington AcrySof IQ Singlepiece IOL with ULTRASERT Delivery System; Lens, Guide, Intraocular Back to Search Results
Model Number AU00T0
Medical Device Problem Codes Device Difficult to Setup or Prepare (1487); Scratched Material (3020)
Health Effect - Clinical Code Insufficient Information (4580)
Date of Event 06/12/2026
Type of Reportable Event Malfunction
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Brand Name
AcrySof IQ Singlepiece IOL with ULTRASERT Delivery System
Common Device Name
Lens, Guide, Intraocular
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 Key50099192
Report Number1119421-2026-01598
Device Sequence Number13263405
Product Code KYB
UDI-Device Identifier00380652394840
UDI-Public(01)00380652394840(17)280520(11)250522(10)16046646
Combination Product (Y/N)N
Initial Reporter CountryIT
PMA/510(K) Number
P930014
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional,Company Representative
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 07/31/2026
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 NumberAU00T0
Device Lot Number16046646
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Initial Date Received by Manufacturer 07/08/2026
Initial Report FDA Received Date07/31/2026
Date Device Manufactured05/22/2025
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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