CUFFLATOR ENDOTRACHEAL TUBE INFLATOR & MONOMETER 8199

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 2013-01-31 for CUFFLATOR ENDOTRACHEAL TUBE INFLATOR & MONOMETER 8199 manufactured by J. T. Posey Co..

Event Text Entries

[3174756] Original report indicates that the request is for service only. The customer reported they want the unit calibrated. Upon receipt and evaluation of the product, it was discovered that the cufflator does not zero. The customer did not provide a date when this was discovered. There was no pt incident or injury reported.
Patient Sequence No: 1, Text Type: D, B5


[10521701] Results: evaluation of the returned unit found that the needle is below zero. Cufflator holds pressure but needle jumps abruptly to 80 when inflating. Needle does not return to zero, instead it returns to its initial position below zero. No readings can be taken since needle jumps abruptly. Note: instructions for use state: before use, the control inflator needs to be checked by closing the connecting piece with the finger, then inflating with inflation bulb to 120 cm h20; value must be constant for 2-3 seconds. If the pressure drops, the device needs repair by the distributor. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2020362-2013-00035
MDR Report Key2982833
Report Source05,06
Date Received2013-01-31
Date of Report2012-12-27
Date Mfgr Received2013-01-22
Date Added to Maude2013-04-17
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
Event Type3
Type of Report3

Device Details

Brand NameCUFFLATOR ENDOTRACHEAL TUBE INFLATOR & MONOMETER
Product CodeBSK
Date Received2013-01-31
Returned To Mfg2013-01-11
Model Number8199
Catalog Number8199
Lot NumberNA
ID NumberNA
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 2013-01-31

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.