Events

Recall of Celsius Thermocool products and Navistar Thermocool products

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Biosense Webster, Inc..

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    32925
  • Event Risk Class
    Class 2
  • Event Number
    Z-0057-06
  • Event Initiated Date
    2005-08-08
  • Event Date Posted
    2005-10-15
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2008-05-23
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=41086
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Cardiac Ablation Percutaneous Catheter - Product Code LPB
  • Reason
    Increased complaints regarding catheters with leaks and flow obstruction.
  • Action
    Urgent letters and response forms dated August 8, 2005 directed consignees to return product.

Device

Celsius Thermocool products and Navistar Thermocool products
  • Model / Serial
    Lots 13027030 to 13044734
  • Product Classification
    Cardiovascular Devices
  • Device Class
    3
  • Implanted device?
    No
  • Distribution
    FL, iL, MA, MI, OH, OK and Belguin, Netherlands, Australia, Japan, Korea, India, Sri Lanka, New Zealand, China, Hong Kong, Singapore, Pakistan, Canada
  • Product Description
    Thermocool Irrigated Catheters || Celsius || LABEL US Part Number# EU CATALOG # || L-1189-01-S D17TCBLRT 35Q-13R PMA; || L-1189-02-S D17TCDLRT 35Q-33R PMA; || L-1189-03-S D17TCFLRT 35Q-53R PMA; || L-1189-04-S D17TCJLRT 35Q-73R PMA; || L-1189-15-S D71TCB5L252RT 35Q-17Q EXPORT; || L-1189-16-S D71TCD5L252RT 35Q-37Q EXPORT; || L-1189-17-S D71TCF5L252FT 35Q-57Q EXPORT; || L-1189-03-S D71TFL252RT 35R-53R EXPORT; || L-1192-03-S D71TFL252RT 35R-53R EXPORT; || L-1192-15-S D71TB5L252RT 35R-17R EXPORT; || L-1192-16-S D7ITD5L252RT 35R-37R EXPORT; || L-1189-02-SI D17TCDLRTI N/A IDE; || L-1189-15-SI D71TCB5L252RTI N/A IDE; || L-1189-16-SI D71TCD5L252RTI N/A IDE; || L-1189-17-SI D71CF5L252RTI N/A IDE || Navistar || LABEL US Part Number# EU CATALOG # || L-1192-17-S D71TF5L252RT 35R-57R EXPORT; || L-1197-14-S NI75TCBH 34H-17M PMA; || L-1197-15-S NI75TCCH 34H-27M PMA; || L-1197-16-S NI75TCDH 34H-37M PMA; || L-1197-17-S NI75TCFH 34H-57M PMA; || L-1197-18-S NI75TCJH 34H-J7M PMA; || L-1208-05-S NS75TBCT252HS 34G-17M PMA; || L-1208-06-S NS75TCCT252HS 34G-27M PMA; || L-1208-07-S NS75TDCT252HS 34G-37M PMA; || L-1208-08-S NS75TFCT252HS 34G-57M PMA; || L-1197-14-SI NI75TCBHI N/A IDE; || L-1197-15-SI NI75TCCHI N/A IDE; || L-1197-16-SI NI75TCDHI N/A IDE; || L-1197-17-SI NI75TCFHI N/A IDE; || L-1197-18-SI NI75TCJHI N/A IDE; || L-1208-05-SI NS75TBCT252HSI N/A IDE; || L-1208-06-SI NS75TCCT252HSI N/A IDE; || L-1208-07-SI NS75TDCT252HSI N/A IDE; || L-1208-08-SI NS75TFCT252HSI N/A IDE
  • Manufacturer
    Biosense Webster, Inc.

Manufacturer

Biosense Webster, Inc.
  • Manufacturer Address
    Biosense Webster, Inc., 15715 Arrow Hwy, Irwindale CA 91706-2006
  • Manufacturer Parent Company (2017)
    Johnson & Johnson
  • Source
    USFDA