• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COOK IRELAND LTD ZILVER PTX 35 DRUG-ELUTING STENT

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

COOK IRELAND LTD ZILVER PTX 35 DRUG-ELUTING STENT Back to Search Results
Model Number G38482
Device Problem Patient Device Interaction Problem (4001)
Patient Problem Reaction to Medicinal Component of Device (4574)
Event Date 09/16/2022
Event Type  Injury  
Manufacturer Narrative
Common device name) niu stent, superficial femoral artery, drug-eluting.
 
Event Description
According to the initial reporter, post a leg angiogram with paclitaxel stent placement procedure, the initial reporter stated that the patient came back in with indurated skin lesions.They wonder if the paclitaxel might be responsible for this.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
ZILVER PTX 35 DRUG-ELUTING STENT
Manufacturer (Section D)
COOK IRELAND LTD
o halloran road
limerick
MDR Report Key15589425
MDR Text Key301599448
Report Number3005580113-2022-00109
Device Sequence Number1
Product Code NIU
UDI-Device Identifier10827002384825
UDI-Public(01)10827002384825(17)240401(10)C1943829
Combination Product (y/n)Y
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Distributor
Reporter Occupation Physician
Type of Report Initial
Report Date 10/12/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/12/2022
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Expiration Date04/01/2024
Device Model NumberG38482
Device Catalogue NumberZISV6-35-125-6-120-PTX
Device Lot NumberC1943829
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? Yes
Distributor Facility Aware Date09/16/2022
Device Age4 MO
Event Location Hospital
Date Report to Manufacturer10/12/2022
Date Device Manufactured05/18/2022
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age48 YR
Patient SexFemale
-
-