Date Initiated by Firm | January 12, 2007 |
Date Posted | March 27, 2007 |
Recall Status1 |
Terminated 3 on June 19, 2008 |
Recall Number | Z-0655-2007 |
Recall Event ID |
37366 |
510(K)Number | K900815 |
Product Classification |
Perfusion System - Product Code DTW
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Product | Terumo Perfusion System 8000 Base, 4 pump, 115v; Model 8000; Catalog No. 16400. |
Code Information |
Hand crank serial numbers 1240 through 1247. |
Recalling Firm/ Manufacturer |
Terumo Cardiovascular Systems Corp 6200 Jackson Rd Ann Arbor MI 48103-9586
|
For Additional Information Contact | 800-521-2818 |
Manufacturer Reason for Recall | The hand crank may crack in the bearing/shaft area due to a manufacturing defect. (Note: Some of the hand cranks subject to this recall were shipped as replacements for hand cranks recalled in the Summer of 2006.) |
FDA Determined Cause 2 | Other |
Action | Consignees were notified by phone between 1/12/07 and 2/23/07 and informed replacement hand cranks would be shipped. |
Quantity in Commerce | 7 |
Distribution | Worldwide, including USA, Belgium, Hong Kong, Japan, Taiwan 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 = DTW
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