LARGE DIAMETER LACRIMAL INTUBATION SET/ STENTUBE OR LACRIMAL LIS052 OR LIS27T *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2006-11-27 for LARGE DIAMETER LACRIMAL INTUBATION SET/ STENTUBE OR LACRIMAL LIS052 OR LIS27T * manufactured by Quest Medical, Inc..

Event Text Entries

[543241] Dr reported that he is experiencing "cheese-wiring" with the stentubes. No samples were saved; no lot numbers were reported. Product code is either lis052 or lis27t.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1649914-2006-00130
MDR Report Key792191
Report Source05,06
Date Received2006-11-27
Date of Report2006-11-27
Date Mfgr Received2006-11-09
Date Added to Maude2006-12-12
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 Location0
Manufacturer ContactMEGAN SIMS
Manufacturer StreetONE ALLENTOWN PARKWAY
Manufacturer CityALLEN TX 75002
Manufacturer CountryUS
Manufacturer Postal75002
Manufacturer Phone9723909800
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLARGE DIAMETER LACRIMAL INTUBATION SET/ STENTUBE OR LACRIMAL
Generic NameMANUAL OPHTHALMIC SURGICAL INSTRUMENT: LACRYMAL PROBE
Product CodeHNW
Date Received2006-11-27
Model NumberLIS052 OR LIS27T
Catalog Number*
Lot NumberUNK
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key779830
ManufacturerQUEST MEDICAL, INC.
Manufacturer AddressONE ALLENTOWN PKWY. ALLEN TX 75002 US
Baseline Brand NameLARGE DIAMETER LACRIMAL INTUBATION SET/ STENTUBE OR LACRIMAL
Baseline Generic NameMANUAL OPHTHALMIC SURGICAL INSTRUMENT: LACRYMAL PROBE
Baseline Model NoLIS052 OR LIS27
Baseline Catalog No*
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
10 2006-11-27

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