Recalls / —
—#64430
Product
Terumo Advanced Perfusion System 1 Central Control Monitor. Terumo Cardiovascular Systems, Ann Arbor, MI; Catalog number 802100. The Central Control Monitor (CCM) provides a centralized display of system information and on-screen control of all system devices. The CCM combines an embedded computer, a touchscreen, and a graphical user interface.
- FDA product code
- DTQ — Console, Heart-Lung Machine, Cardiopulmonary Bypass
- Device class
- Class 2
- Medical specialty
- Cardiovascular
- 510(k) numbers
- K022947
- Affected lot / code info
- Serial numbers 0020 through 0980.
Why it was recalled
The monitor may exhibit start-up failure, video/display issues, calibration issues, and partial or complete loss of functionality during use.
Root cause (FDA determination)
Device Design
Action the firm took
Consignees were notified via an Urgent Medical Device Correction: Safety Advisory letter dated 1/12/09 advised of the reason for the correction, potential problems, and provided clinical information should the problem(s) arise. Customers are to review the notice, assure that all users are aware of the notice, and confirm receipt of the communication by completing the attached Customer Response Form and faxing it to the number indicated on the form. Questions or concerns should be directed to Terumo CVS Customer Service at 1-800-521-2818.
Recalling firm
- Firm
- Terumo Cardiovascular Systems Corporation
- Address
- 6200 Jackson Road, Ann Arbor, Michigan 48103-9586
Distribution
- Distribution pattern
- Worldwide Distribution -- USA, Australia, Belgium, Canada, Dominican Republic, Egypt, Germany, Honduras, Hong Kong, India, Indonesia, Japan, Jordan, Kuwait, Malaysia, Mexico, Pakistan, Philippines, Russia, Saudi Arabia, Singapore, South Africa, South Korea, Taiwan, Thailand, Turkey, United Arab Emirates, and Viet Nam.
Timeline
- Recall initiated
- 2009-01-12
- Posted by FDA
- 2009-05-29
- Terminated
- 2009-07-14
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #64430. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.