ALCON MICROSURGICAL INSTRUMENTS, CANNULA OPHTHALMIC

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-03 for ALCON MICROSURGICAL INSTRUMENTS, CANNULA OPHTHALMIC manufactured by Alcon Research, Llc - Alcon Precision Device.

Event Text Entries

[181793812] No sample or lot number information has been received by manufacturing for evaluation. 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).
Patient Sequence No: 1, Text Type: N, H10


[181793813] A physician reported that the soft tip from a soft tip cannula that was used during a previous vitrectomy surgery was detected during a one year post operative gonioscopy exam to have detached and retained inside of the patient's right eye. The patient complained of chronic edema and lack of visual acuity and was treated with steroid drops of durezol, combigan and simbrinza to treat vitritis. The detached soft tip was subsequently removed from the patient's eye during a cataract procedure.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2523835-2020-00056
MDR Report Key9780899
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-03
Date of Report2020-03-03
Date Mfgr Received2020-02-21
Date Added to Maude2020-03-03
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. JONATHAN SCHLECH
Manufacturer Street6201 SOUTH FREEWAY MAIL STOP AB2-6
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal76134
Manufacturer Phone8175514979
Manufacturer G1ALCON RESEARCH, LLC - ALCON PRECISION DEVICE
Manufacturer Street714 COLUMBIA AVENUE
Manufacturer CitySINKING SPRING PA 19608
Manufacturer CountryUS
Manufacturer Postal Code19608
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameALCON MICROSURGICAL INSTRUMENTS, CANNULA OPHTHALMIC
Generic NameCANNULA, OPHTHALMIC
Product CodeHMX
Date Received2020-03-03
Model NumberNA
Catalog NumberASKU
Lot NumberASKU
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALCON RESEARCH, LLC - ALCON PRECISION DEVICE
Manufacturer Address714 COLUMBIA AVENUE SINKING SPRING PA 19608 US 19608


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-03

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