UNIVERSAL PICC CATHETER SECUREMENT 3300MWA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2018-09-27 for UNIVERSAL PICC CATHETER SECUREMENT 3300MWA manufactured by Tidi Products, Llc.

Event Text Entries

[122659265] This report is being submitted as a result of a remediation capa to reassess product risks. No further actions will be taken. All complaints are trended and reviewed by management on a monthly basis. As part of this monthly review, any excursion above the control limits for this failure mode will be assessed, documented and acted upon as warranted. Manufacturer reference file # (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[122659266] Customer reported the glue strip is constantly delaminating from the lid, leaving the strip over the picc line. The top adhesive is peeling off of the loop and staying stuck to the catheter. It is unknown when the issue was discovered and no patient incident or injury was reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2182318-2018-00011
MDR Report Key7914972
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2018-09-27
Date of Report2018-09-24
Date of Event2016-10-12
Date Mfgr Received2018-09-24
Device Manufacturer Date2016-08-04
Date Added to Maude2018-09-27
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 ContactJACKIE KRIEGLSTEIN
Manufacturer Street570 ENTERPRISE DRIVE
Manufacturer CityNEENAH WI 54956
Manufacturer CountryUS
Manufacturer Postal54956
Manufacturer Phone9207514300
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUNIVERSAL PICC CATHETER SECUREMENT
Generic NameGRIP-LOK 3300MWA
Product CodeKMK
Date Received2018-09-27
Model Number3300MWA
Catalog Number3300MWA
Lot Number25607960
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTIDI PRODUCTS, LLC
Manufacturer Address570 ENTERPRISE DRIVE NEENAH WI 54956 US 54956


Patients

Patient NumberTreatmentOutcomeDate
10 2018-09-27

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