MONARCH III IOL DELIVERY SYSTEM, CARTRIDGE D 8065977763

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2020-02-04 for MONARCH III IOL DELIVERY SYSTEM, CARTRIDGE D 8065977763 manufactured by Alcon Research, Llc - Huntington.

Event Text Entries

[181931614] A sample device was not returned for analysis. Complaint history and product history records were reviewed and documentation indicated the product met release criteria. The lens model/diopter used was not a correct combination and is only qualified for two specific cartridge models. Root cause has not been identified. There have been no other complaints reported in the lot number. The manufacturer internal reference number is: (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[181931615] An inventory specialist reported that during an intraocular lens (iol) implant procedure, the cartridge bent and cracked the haptic of the lens. The procedure was completed with a new lens and cartridge. There was patient contact, but no patient harm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1119421-2020-00178
MDR Report Key9665350
Report SourceOTHER
Date Received2020-02-04
Date of Report2020-02-04
Date of Event2019-10-07
Date Mfgr Received2020-01-07
Device Manufacturer Date2019-04-30
Date Added to Maude2020-02-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. JASON MICHAELIDES
Manufacturer Street6201 SOUTH FREEWAY MAIL STOP AB2-6
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal76134
Manufacturer Phone8175686438
Manufacturer G1ALCON RESEARCH, LLC - HUNTINGTON
Manufacturer Street6065 KYLE LANE
Manufacturer CityHUNTINGTON WV 25702
Manufacturer CountryUS
Manufacturer Postal Code25702
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameMONARCH III IOL DELIVERY SYSTEM, CARTRIDGE D
Generic NameFOLDERS AND INJECTORS, INTRAOCULAR LENS (IOL)
Product CodeMSS
Date Received2020-02-04
Model NumberNA
Catalog Number8065977763
Lot Number32710539
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALCON RESEARCH, LLC - HUNTINGTON
Manufacturer Address6065 KYLE LANE HUNTINGTON WV 25702 US 25702


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-04

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