FORM FIT HYDROGEL CANALICULAR PLUG 6303

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2011-01-07 for FORM FIT HYDROGEL CANALICULAR PLUG 6303 manufactured by Oasis Medical, Inc..

Event Text Entries

[1789284] Reported observation: pt developed canaliculitis after insertion of an oasis medical form fit hydrogel canalicular plug. (b)(4). Product lot number: unk. Product inserted on: unk. Date of complication: reported to oasis medical, inc on (b)(6) 2010. Attending doctor successfully irrigated the plug from the canaliculus. Pt treated with an antibiotic treatment.
Patient Sequence No: 1, Text Type: D, B5


[8870548] The device was not returned for eval. Specific product lot info was not provided with the initial report of the complications. The date of plug insertion and removal was not reported with the initial report of complications. The attending doctor was able to irrigate the plug from the canaliculus. A request for case specific info has been requested from the reporting doctor. Supplemental info will be submitted when received.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2083373-2010-00003
MDR Report Key1960247
Report Source05
Date Received2011-01-07
Date of Report2011-01-07
Date of Event2009-12-10
Date Mfgr Received2010-12-10
Date Added to Maude2012-02-29
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 FDA0
Event Location0
Manufacturer ContactNICOLA HUBERT, MGR.
Manufacturer Street514 S. VERMONT AVE.
Manufacturer CityGLENDORA CA 91741
Manufacturer CountryUS
Manufacturer Postal91741
Manufacturer Phone6268525182
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameFORM FIT HYDROGEL CANALICULAR PLUG
Generic NameINTRACANALICULAR PLUG
Product CodeLZU
Date Received2011-01-07
Model Number6303
Catalog Number6303
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerOASIS MEDICAL, INC.
Manufacturer Address514 S. VERMONT AVE. GLENDORA CA 91741 US 91741


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2011-01-07

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