SILIKON 1000 OIL 8065601187

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2018-12-05 for SILIKON 1000 OIL 8065601187 manufactured by Alcon Laboratories, Inc..

Event Text Entries

[129384022] 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


[129384023] A customer reported that following a vitreoretinal procedure, 2-3 days postoperatively, it was found that the ophthalmic liquid and oil remained in the patient's eye. An additional procedure was preformed in order to remove the liquid and gas. Additional information has been requested. This is two of two reports filed for this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1610287-2018-00050
MDR Report Key8134847
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2018-12-05
Date of Report2019-01-31
Date Mfgr Received2019-01-29
Date Added to Maude2018-12-05
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 ContactMS. CINDY MILAM
Manufacturer Street6201 SOUTH FREEWAY MAIL STOP AB2-6
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal76134
Manufacturer Phone8176152231
Manufacturer G1ALCON LABORATORIES, INC.
Manufacturer Street6201 SOUTH FREEWAY
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal Code76134
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameSILIKON 1000 OIL
Generic NameFLUID, INTRAOCULAR
Product CodeLWL
Date Received2018-12-05
Model NumberNA
Catalog Number8065601187
Lot NumberASKU
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALCON LABORATORIES, INC.
Manufacturer Address6201 SOUTH FREEWAY FORT WORTH TX 76134 US 76134


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-12-05

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