ENDOTRACHEAL TUBE INFLATOR AND MANOMETER 8199

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 2012-12-11 for ENDOTRACHEAL TUBE INFLATOR AND MANOMETER 8199 manufactured by J. T. Posey Co..

Event Text Entries

[3372069] Customer reported that the unit needs calibration. No pt incident or injury was reported.
Patient Sequence No: 1, Text Type: D, B5


[10355355] Evaluation results: - evaluation of the returned unit found that the reported issue cannot be confirmed. Needle moves up when inflation bulb is squeezed and holds pressure but needle does not reset to zero. No readings taken since needle does not reset to zero. Note: instructions for use state: the cufflator should be calibrated annually, or if measurements fall outside of this range, or if the cufflator needle does not indicate a reading of zero when nothing is connected, or if the unit is ever dropped. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2020362-2012-00679
MDR Report Key2919616
Report Source06
Date Received2012-12-11
Date of Report2012-11-26
Date Mfgr Received2012-12-06
Date Added to Maude2013-03-15
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 ContactROXANA KOUSSA
Manufacturer Street5635 PECK RD.
Manufacturer CityARCADIA CA 91006
Manufacturer CountryUS
Manufacturer Postal91006
Manufacturer Phone6264433143
Manufacturer G1J. T. POSEY CO.
Manufacturer Street5635 PECK RD.
Manufacturer CityARCADIA CA 91006
Manufacturer CountryUS
Manufacturer Postal Code91006
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameENDOTRACHEAL TUBE INFLATOR AND MANOMETER
Product CodeBSK
Date Received2012-12-11
Model Number8199
Catalog Number8199
Lot NumberIML
ID NumberMA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerJ. T. POSEY CO.
Manufacturer AddressARCADIA CA US


Patients

Patient NumberTreatmentOutcomeDate
10 2012-12-11

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