| Class 2 Device Recall | |
Date Initiated by Firm | May 06, 2004 |
Date Posted | November 03, 2004 |
Recall Status1 |
Terminated 3 on June 29, 2010 |
Recall Number | Z-0168-05 |
Recall Event ID |
30218 |
Product Classification |
Heart-Valve, Allograft - Product Code MIE
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Product | CryoValve, Aortic Valve |
Code Information |
Donor #46496, Serial #6741341, Model #AV10 |
Recalling Firm/ Manufacturer |
Cryolife Inc 1655 Roberts Blvd Nw Kennesaw GA 30144-3632
|
For Additional Information Contact | Mr. P. Tyler Cochran, CQA, CTBS 770-419-3355 |
Manufacturer Reason for Recall | CryoLife conducted a retrospective review which revealed the sterilization cycle of instruments used during processing of various tissues could not be confirmed as acceptable. |
FDA Determined Cause 2 | Other |
Action | Consignees were notified by letter on/about May 6, 2004. |
Quantity in Commerce | 1 unit |
Distribution | Nationwide, Austria, Canada, Germany |
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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