LARGE DIAMETER LACRIMAL INTUBATION SET/STENTUBE LIS052 *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2006-04-12 for LARGE DIAMETER LACRIMAL INTUBATION SET/STENTUBE LIS052 * manufactured by Quest Medical, Inc..

Event Text Entries

[446676] The customer reported that during a dcr procedure, the stentube broke. Another stentube was used and there were no pt complicatins reported. The product was not saved for evaluation. The product code is lis052, lot number 25745.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1649914-2006-00033
MDR Report Key700539
Report Source06
Date Received2006-04-12
Date of Report2006-03-30
Date of Event2006-03-15
Date Mfgr Received2006-03-15
Device Manufacturer Date2005-11-01
Date Added to Maude2006-04-19
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 ContactKATHRYN JAYNE
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
Generic NameMANUAL OPHTHALMIC SURGICAL INSTRUMENT: LACRYMAL PROBE
Product CodeHMW
Date Received2006-04-12
Model NumberLIS052
Catalog Number*
Lot Number25745
ID Number*
Device Expiration Date2007-10-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key689629
ManufacturerQUEST MEDICAL, INC.
Manufacturer AddressONE ALLENTOWN PKWY. ALLEN TX 75002 US
Baseline Brand NameSTENTUBE
Baseline Generic NameOPHTHALMIC INTUBATION TUBE
Baseline Model NoLIS052
Baseline Catalog NoLIS052
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
10 2006-04-12

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