Events

Recall of Device Recall Terumo

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Terumo Cardiovascular Systems Corp.

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
    32923
  • Event Risk Class
    Class 2
  • Event Number
    Z-0140-06
  • Event Initiated Date
    2005-07-26
  • Event Date Posted
    2005-11-16
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2006-05-02
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=41081
  • 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
    Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type - Product Code KFM
  • Reason
    Small cracks in the blood chamber may allow air to enter the rotor of the device.
  • Action
    Terumo notified consignees by telephone on 7/26/05 and followed by letter dated 7/28/05. Accounts are requested to return product.

Device

Device Recall Terumo
  • Model / Serial
    Convenience Kit Identifier Code/Kit Lot Numbers: 65077 FA17 62266-01 EP13 62266-01 FA31 63819-01 FC07 64034 FA03 64033 FD07 70131 FA03 70131 FA10 63607 FA31 63607 FD07 64091 FC07 64338 EP13 64338 FC07 70964 EP20 70964 FD07 70014-02 EP13 70014-02 FA03 70014-02 FC07 70014-02 FC07T 70014-02 FD07 70226-01 FD07 64987 FA24 64987 FD14 62933-01 FD14 62984-01 FA24 63004-01 FA03 63004-01 FA24 63361-01 EP27 63118 EP13 63118-01 FA24 63118-01 FC28 63118-01 FD14
  • Product Classification
    Cardiovascular Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    AZ, CA, KY, IL, LA, MD, WA , WI
  • Product Description
    Terumo/Capiox Cardiovascular Kit containing the CAPIOX Disposable Centrifugal Pump || The centrifugal pump is designated as TCVS Product Code 1ZZ*SP45A. The devices are assembled with PVC tubing and other devices according to individual customer specifications and then packaged into Custom Cardiovascular Procedure Kits (Convenience Kits) as follows: || Convenience Kit Identifier Code/Kit Lot Numbers: || 65077 FA17 || 62266-01 EP13 || 62266-01 FA31 || 63819-01 FC07 || 64034 FA03 || 64033 FD07 || 70131 FA03 || 70131 FA10 || 63607 FA31 || 63607 FD07 || 64091 FC07 || 64338 EP13 || 64338 FC07 || 70964 EP20 || 70964 FD07 || 70014-02 EP13 || 70014-02 FA03 || 70014-02 FC07 || 70014-02 FC07T || 70014-02 FD07 || 70226-01 FD07 || 64987 FA24 || 64987 FD14 || 62933-01 FD14 || 62984-01 FA24 || 63004-01 FA03 || 63004-01 FA24 || 63361-01 EP27 || 63118 EP13 || 63118-01 FA24 || 63118-01 FC28 || 63118-01 FD14
  • Manufacturer
    Terumo Cardiovascular Systems Corp

Manufacturer

Terumo Cardiovascular Systems Corp
  • Manufacturer Address
    Terumo Cardiovascular Systems Corp, 6200 Jackson Rd, Ann Arbor MI 48103-9586
  • Source
    USFDA