TRANSTAR 84 IN SINGLE MONITORING KIT MX9505T

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 2010-10-21 for TRANSTAR 84 IN SINGLE MONITORING KIT MX9505T manufactured by Smiths Medical Asd, Inc.,.

Event Text Entries

[1755952] The reporter stated that the device tubing separated. There was no reported patient injury or treatment associated with this event.
Patient Sequence No: 1, Text Type: D, B5


[8852816] (b)(4). Customer has not yet returned the device to the manufacturer for device evaluation. When and if the device becomes available and is returned and evaluated the manufacturer will file a follow-up report detailing the results of the evaluation.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2183502-2010-00464
MDR Report Key1882476
Report Source06
Date Received2010-10-21
Date of Report2010-10-19
Date of Event2010-09-21
Date Facility Aware2010-09-21
Report Date2010-10-19
Date Reported to FDA2010-10-19
Date Mfgr Received2010-09-21
Device Manufacturer Date2009-04-01
Date Added to Maude2010-12-27
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 Location3
Manufacturer ContactPETE HIRTE
Manufacturer Street1265 GREY FOX ROAD
Manufacturer CityST. PAUL MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone6516287384
Manufacturer G1SMITHS MEDICAL ASD
Manufacturer Street6250 SHIER-RINGS ROAD
Manufacturer CityDUBLIN OH 43016
Manufacturer CountryUS
Manufacturer Postal Code43016
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRANSTAR 84 IN SINGLE MONITORING KIT
Generic NamePRESSURE MONITORING SET
Product CodeDPT
Date Received2010-10-21
Model NumberNA
Catalog NumberMX9505T
Lot Number1570984
ID NumberNA
Device Expiration Date2012-04-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age17 MO
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC.,
Manufacturer AddressDUBLIN OH US


Patients

Patient NumberTreatmentOutcomeDate
10 2010-10-21

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