Events

Recall of Device Recall Arrow International, Inc. Intraaortic balloon catheter

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Arrow International, 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
    51080
  • Event Risk Class
    Class 1
  • Event Number
    Z-1212-2009
  • Event Initiated Date
    2009-02-02
  • Event Date Posted
    2009-04-16
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2010-07-06
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=78463
  • 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
    Intra-aortic balloon and control system - Product Code DSP
  • Reason
    A fault in the connector of the pump tubing assembly may result in the volume setting on the pump defaulting to 2.5 ccs or 5 ccs (depending on iabp model) rather than the appropriate 30, 40, or 50 cc volume.
  • Action
    An "Urgent Medical Device Recall" letter dated February 2, 2009 was issued to consignees via US Certified Mail to notify users of the problem. Users were instructed to check their inventory for the affected products, quarantine, and return the them to Arrow International, Inc. Customers were also instructed to follow the "Mitigation Directions" in circumstances where alternate Intra-Aortic Balloon (IAB) catheters/adaptors or other forms of therapy are not available (until receipt of available product). Canadian accounts were notified on February 9, 2009 by courier and International accounts notified on 6 February 2009 and 10 February 2009 via Registered Post/UPS. Direct questions to your local Sales Representative or the Arrow International Customer Service at 1-800-523-8446 (US) or 1-919-361-4062 (outside US). Press Release issued April 13, 2009 is posted to firm's webiste: http://www.arrowintl.com/iab_recall.asp.

Device

Device Recall Arrow International, Inc. Intraaortic balloon catheter
  • Model / Serial
    Lot/Serial Numbers: MF6122058 MF7065640 MF7076257 MF7076378 MF7097392 MF7118003 MF7118004 MF7118219 MF7128387 MF7128471 MF7128504 MF7128505 MF8018907 MF8018997 MF8030122 MF8039664 MF8039878 MF8040324 MF8040325 MF8040638 MF8050911 MF8061125 MF8061176 MF8061334 MF8061500 MF8061615 MF8071782 MF8072074 MF8082267 MF8082584 MF8092783 MF8092784 MF8093000 MF8093001 MF8103155 MF8103262 MF8103263 MF8124064 MF8124178 MF8124064 MF8124307 and MF8124408.
  • Product Classification
    Cardiovascular Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution: USA, Argentina, Australia, Taiwan, Singapore, New Zealand, India, Brazil, Belgium, Korea, Peru, Finland, and Denmark.
  • Product Description
    8 Fr 30cc Ultra 8 IAB, || IAB-05830-U, Intra-aortic balloon catheter. || The Intra-aortic balloon (IAB) is utilized for IAB counter-pulsation therapy, whereby balloon inflation in the aorta during diastole and deflation during systole increase blood supply to the heart muscle and decrease work of the left ventricle.
  • Manufacturer
    Arrow International, Inc.

Manufacturer

Arrow International, Inc.
  • Manufacturer Address
    Arrow International, Inc., 9 Plymouth St, Everett MA 02149-1814
  • Manufacturer Parent Company (2017)
    Teleflex Incorporated
  • Source
    USFDA