| Class 2 Device Recall Terumo Advanced Perfusion System 1 | |
Date Initiated by Firm | September 10, 2007 |
Date Posted | December 01, 2007 |
Recall Status1 |
Terminated 3 on February 23, 2008 |
Recall Number | Z-0321-2008 |
Recall Event ID |
38466 |
510(K)Number | K022947 |
Product Classification |
Perfusion System - Product Code DTQ
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Product | Terumo Advanced Perfusion System, 1 Roller Pump, 4 inch diameter; Catalog No. 801040, Terumo Cardiovascular Systems, Ann Arbor, MI 48103 |
Code Information |
Serial Numbers 2110 through 2125. |
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 | Failure to operate; The pump may fail to operate, and be difficult to hand crank, due to an internal electrical short condition. |
FDA Determined Cause 2 | Process control |
Action | Consignees were notified via an Urgent Medical Device Correction letter dated 9/10/07, which provided them guidance in the event the problem occurs and advised them they would be contacted to schedule replacement of the circuit boards. |
Quantity in Commerce | 16 |
Distribution | Worldwide Distribution-USA including states of Alabama, Arizona, Florida, Illinois, Indiana, Mississippi, Nebraska, North Carolina, Pennsylvania, and Virginia, and countries of Belgium, Hong Kong 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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