| Class 3 Device Recall Terumo APS 1 | |
Date Initiated by Firm | May 01, 2004 |
Date Posted | December 27, 2006 |
Recall Status1 |
Terminated 3 on February 01, 2007 |
Recall Number | Z-0311-2007 |
Recall Event ID |
36398 |
510(K)Number | K022947 |
Product Classification |
cardiovascular perfusion system - Product Code DTQ
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Product | Terumo Advanced Perfusion System 1; 100V -120V, 15 A (circuit breaker), 50/60 Hz (20A power source required) base; Model 801763. |
Code Information |
Serial numbers 0011 through 0039 and 0041 through 0170. |
Recalling Firm/ Manufacturer |
Terumo Cardiovascular Systems Corp 6200 Jackson Rd Ann Arbor MI 48103-9586
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For Additional Information Contact | 800-521-2818 |
Manufacturer Reason for Recall | The battery status light on the front panel may not accurately reflect the actual status of the battery. The battery may contain more charge than indicated. |
FDA Determined Cause 2 | Other |
Action | U.S. consignees were visited and new software installed between May 2004 and November 2005. Currently, approximately 50% of exported units have been upgraded. |
Quantity in Commerce | 159 |
Distribution | Worldwide, including USA, Belgium, Canada, China, Egypt, Germany, India, Indonesia, Japan, Malaysia, Pakistan, Republic of China, Singapore, South Africa, South Korea and United Arab Emirates. |
Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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510(K) Database | 510(K)s with Product Code = DTQ
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