Date Initiated by Firm | January 23, 2004 |
Date Posted | March 18, 2005 |
Recall Status1 |
Terminated 3 on July 22, 2006 |
Recall Number | Z-0632-05 |
Recall Event ID |
30919 |
510(K)Number | K001981 |
Product Classification |
System, Test, Anticardiolipin Immunological - Product Code MID
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Product | DiaSorin Anti-Cardiolipin IgA ELISA kit for the detection in human serum or plasma of antoantibodies specific for Cardiolipin IgA. Catalog No.: 7800. Manufactured for DiaSorin Inc., 1951 Northwestern Avenue, Stillwater, MN 55082-0285 |
Code Information |
catalog # 7800, lot # 039229, expiration date 12/23/04 |
Recalling Firm/ Manufacturer |
Diasorin Inc. 1951 Northwestern Ave S Stillwater MN 55082-7536
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For Additional Information Contact | DiaSorin Technical Services 800-328-1482 |
Manufacturer Reason for Recall | DiaSorin Anti-Cardiolipin IgA kit's positive control is out of acceptable limits. |
FDA Determined Cause 2 | Other |
Action | Customers were notified via a letter which described the product and the problem. Recommended to destroy all affected kits and stated that the kits will be replaced. |
Quantity in Commerce | 16 kits |
Distribution | GA, NY & KS |
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 = MID
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