HUDSON RCI BITE GARD MOLAR BITE BLOCK 1140

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2011-05-19 for HUDSON RCI BITE GARD MOLAR BITE BLOCK 1140 manufactured by Teleflex Medical.

Event Text Entries

[15535256] The event is reported as: complaint alleges that the green wings on the device disconnected from the block while the pt was under anesthesia. None of the pieces that came off went into the pt's mouth. All the pieces were retrieved. No pt injury reported.
Patient Sequence No: 1, Text Type: D, B5


[15942261] Sample has not been received by manufacturer in time for this report. Investigation incomplete. A follow-up investigation report will be sent when completed.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3004365956-2011-00198
MDR Report Key2109975
Report Source05,07
Date Received2011-05-19
Date of Report2011-04-27
Date of Event2011-04-16
Date Mfgr Received2011-04-27
Device Manufacturer Date2011-01-01
Date Added to Maude2012-03-23
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactELAINE BURKLE, RN
Manufacturer StreetPO BOX 12600
Manufacturer CityDURHAM NC 27709
Manufacturer CountryUS
Manufacturer Postal27709
Manufacturer Phone9194334957
Manufacturer G1TELEFLEX
Manufacturer StreetAVE. TRANSFORMACION 5954 PARQUE INDUSTRIAL FINSA
Manufacturer CityNUEVO LAREDO 88275
Manufacturer CountryMX
Manufacturer Postal Code88275
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameHUDSON RCI BITE GARD MOLAR BITE BLOCK
Generic NameBITE GUARD MOLAR
Product CodeJXL
Date Received2011-05-19
Model NumberNA
Catalog Number1140
Lot Number02A1101331
ID NumberNA
OperatorOTHER
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressNUEVO LAREDO MX


Patients

Patient NumberTreatmentOutcomeDate
10 2011-05-19

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