Date Initiated by Firm | February 15, 2007 |
Date Posted | March 13, 2007 |
Recall Status1 |
Terminated 3 on May 08, 2007 |
Recall Number | Z-0594-2007 |
Recall Event ID |
37356 |
510(K)Number | K993276 |
Product Classification |
D-dimer, in vitro diagnostic - Product Code GHH
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Product | Clearview Simplify D-dimer, in vitro diagnostic for qualitative detection of D-dimer in human whole blood and plasma.
Product No. 61100KVC
10 test devices containing anti D-dimer monoclonal antibody and sheep anti-mouse antibody 1 x 2.6 mL buffer containing 0.9% sodium chloride and 0.05% sodium azide
10 plastic pipettes
Wampole Laboratories
Inverness Medical Professional diagnostics group Manufactured by Agen Biomedical Ltd, Brisbane, QLD Australia. |
Code Information |
Kit lot number: PX018A Test device batch number: 682-024 Catalog Number: 6100KVC Expiration date: 3/2008 |
Recalling Firm/ Manufacturer |
Inverness Medical Professional Diagnostics 2 Research Way Princeton NJ 08540-6628
|
For Additional Information Contact | Katrina Fielder 609-627-8038 |
Manufacturer Reason for Recall | Lot PX018A is exhibiting a decrease in sensitivity affecting the qualitative result around the cut off. |
FDA Determined Cause 2 | Other |
Action | Recall notification letters were sent to all customers on 2/14/07 by first class mail. |
Quantity in Commerce | 382 kits |
Distribution | Worldwide, including USA, Puerto Rico, and Canada. |
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 = GHH
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