DIALYSIS UNKNOWN

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,06 report with the FDA on 2012-06-20 for DIALYSIS UNKNOWN manufactured by Covidien.

Event Text Entries

[18206097] 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


[18279900] It was reported to covidien on (b)(6) 2012 that a customer had an issue with a dialysis catheter. The customer stated that there was a leak between the exit site and the hub. The patient has had a palindrome in place for at least 12 months. The catheter was removed and replaced.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1317749-2012-00131
MDR Report Key2629682
Report Source01,06
Date Received2012-06-20
Date of Report2012-05-31
Date of Event2012-05-31
Report Date2012-05-31
Date Reported to Mfgr2012-05-31
Date Mfgr Received2012-05-31
Date Added to Maude2012-10-15
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 ContactJILL SARAIVA
Manufacturer Street15 HAMPSHIRE ST.
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5084524970
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 NameDIALYSIS UNKNOWN
Generic NameDIALYSIS CATHETER
Product CodeNYU
Date Received2012-06-20
Model NumberUNK
Catalog NumberUNK
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address5439 STATE ROUTE 40 ARGYLE NY 12809 US 12809


Patients

Patient NumberTreatmentOutcomeDate
10 2012-06-20

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