Date Initiated by Firm |
September 29, 2005 |
Date Posted |
November 01, 2005 |
Recall Status1 |
Terminated 3 on January 29, 2007 |
Recall Number |
Z-0113-06 |
Recall Event ID |
33707 |
PMA Number |
P980018 |
Product Classification |
System, Test, Her-2/Neu, Ihc - Product Code MVC
|
Product |
K 520411-2, Hercep Test, 35Test, HER2, Protein |
Code Information |
Lot number: 00016943 |
Recalling Firm/ Manufacturer |
Dakocytomation California Inc 6392 Via Real Carpinteria CA 93013-2921
|
For Additional Information Contact |
Scot D. Kinghorn 805-566-5478
|
Manufacturer Reason for Recall |
Formulation error in the Visualization Reagent (vial 3) component contained in Hercep Test kits. The error was in the concentration of Polyethylene Glycol contained in the formulation.
|
FDA Determined Cause 2 |
Other |
Action |
Notification letter dated Sept 29,2005 was sent by certified mail to consignees instructing disposal of product. |
Quantity in Commerce |
545 |
Distribution |
Nationwide |
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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PMA Database |
PMAs with Product Code = MVC and Original Applicant = Agilent Technologies Singapore (International) Pte Ltd.
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