FDA Logo links to FDA home pageCenter for Devices and Radiological Health, U.S. Food and Drug AdministrationHHS Logo links to Department of Health and Human Services website

FDA Home Page | CDRH Home Page | Search | CDRH A-Z Index | Contact CDRH U.S. Food and Drug Administration Center for Devices and Radiological Health [Skip navigation]
horizonal rule
Super Search
510(k) | Registration & Listing | Adverse Events | PMA | Classification | CLIA
CFR Title 21 | Advisory Committees | Assembler | Recalls | Guidance | Standards
 

 

Adverse Event Report

BAXTER HEALTH CARE CORP T-CONNECTOR EXTENSION SET   back to search results
Catalog Number 2N3326
Event Description

The t-connector for the interlink injection system will not flush. May be plugged.

 
Search Alerts/Recalls

  new search  |  submit an adverse event report

Type of DeviceT-CONNECTOR EXTENSION SET
Baseline Device 510(K) Number
Baseline Device PMA Number
Manufacturer (Section D)
BAXTER HEALTH CARE CORP
rt 120 & wilson
round lake IL 60073
Device Event Key344991
MDR Report Key355768
Event Key335226
Report NumberMW1023090
Device Sequence Number1
Product CodeFPA
Report Source Voluntary
Report Date 09/28/2001
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received10/11/2001
Is This An Adverse Event Report? No
Is This A Product Problem Report? Yes
Device Operator Health Professional
Device Catalogue Number2N3326
Device LOT NumberU574608
Was Device Available For Evaluation? Yes
Is the Device an Implant? No
Is this an Explanted Device? No Answer Provided

Database last updated on February 28, 2009

horizonal rule

CDRH Home Page | CDRH A-Z Index | Contact CDRH | Accessibility | Disclaimer
FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA | HHS Home Page

Center for Devices and Radiological Health / CDRH