QPLUS CDC+ SE TRAY 13.5F X 16CM 8888135167

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 2012-09-19 for QPLUS CDC+ SE TRAY 13.5F X 16CM 8888135167 manufactured by Covidien.

Event Text Entries

[18974183] It was reported to covidien on (b)(6) 2012 that a customer had an issue with a dialysis catheter. The customer states the catheter was inserted and in use for 2-3 days. Upon start of the crrt, the catheter began pulling in air and leaking blood from the catheter extension tubing. The catheter was pulled and replaced.
Patient Sequence No: 1, Text Type: D, B5


[19219027] Submit date: (b)(4) 2012. An investigation is currently underway. Upon completion, the results will be forwarded.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1317749-2012-00214
MDR Report Key2763141
Report Source05,06
Date Received2012-09-19
Date of Report2012-08-23
Date of Event2012-08-23
Report Date2012-08-23
Date Reported to Mfgr2012-08-23
Date Mfgr Received2012-08-23
Date Added to Maude2012-11-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location3
Manufacturer ContactEDWARD ALMEIDA
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5084524151
Manufacturer G1COVIDIEN
Manufacturer Street5439 STATE ROUTE 40
Manufacturer CityARGYLE NY 12809
Manufacturer CountryUS
Manufacturer Postal Code12809
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameQPLUS CDC+ SE TRAY 13.5F X 16CM
Generic NameDIALYSIS CATHETER
Product CodeNYU
Date Received2012-09-19
Model Number8888135167
Catalog Number8888135167
Lot NumberUNKNOWN
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeNA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address5439 STATE ROUTE 40 ARGYLE NY 12809 US 12809


Patients

Patient NumberTreatmentOutcomeDate
10 2012-09-19

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