| Class 2 Device Recall Terumo APS 1 | |
Date Initiated by Firm | October 16, 2006 |
Date Posted | February 14, 2007 |
Recall Status1 |
Terminated 3 on July 07, 2009 |
Recall Number | Z-0433-2007 |
Recall Event ID |
36490 |
510(K)Number | K022947 |
Product Classification |
Perfusion System - Product Code DTQ
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Product | Terumo Advanced Perfusion System 1; 220V -240V, 7A (circuit breaker), 50/60 Hz (10A power source required) base; Model 801764. (Not distributed within the United States). |
Code Information |
Serial numbers 0006 through 0066 and 0100 through 0245. |
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 | A 'battery needs service' message may be displayed, or the remaining battery time may incorrectly become zero, even when the battery is fully functional. |
FDA Determined Cause 2 | Other |
Action | Consignees were sent a letter dated 11/10/06 informing them of the nature of the issues and that the firm would contact them to schedule a service call to install the software upgrade package. The software upgrade installation began at customers on 10/16/06, prior to issuance of the letter to consignees. |
Quantity in Commerce | 207 |
Distribution | Worldwide distribution ---- including USA and countries Australia, Belgium, Canada, China, Dominican Republic, Egypt, Germany, India, Indonesia, Japan, Malaysia, Mexico, Pakistan, Republic of China, Singapore, South Africa, South Korea, Thailand 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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