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U.S. Department of Health and Human Services

Class 2 Device Recall FastPack Free T4 Immunoassay

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 Class 2 Device Recall FastPack Free T4 Immunoassay see related information
Date Posted December 19, 2013
Recall Status1 Terminated on September 18, 2014
Recall Number Z-0549-2014
Recall Event ID 66842
510(K)Number K030329 
Product Classification Radioimmunoassay, free thyroxine - Product Code CEC
Product FastPack Free T4 Immunoassay
Chemilunescence assay for the determination of Free T4


The FastPack free T4 Immunoassay is a paramagnetic particle immunoassay for the in vitro quantitative determination of FT4 in human serum. The FastPack free T4 Immunoassay is designed for use with the FastPack System.
Code Information Testosterone. Catalog Number 25000043. Lot Number 1310028-2P.Exp Date: 4/10/2014
Recalling Firm/
Manufacturer
Qualigen Inc
2042 Corte del Nogal
Carlsbad CA 92011-1438
760-918-9165
For Additional Information Contact
760-918-9165
Manufacturer Reason
for Recall
Qualigen initiated this recall because the FastPack kit may cause lower than expected results due to a manufacturing defect.
FDA Determined
Cause 2
Process change control
Action Qualigen, Inc., notified customers of the recall by calling customers via telephone (with a telephone script) on 11/08/2013. The telephone (script) included the reason for recall, product description with codes, instructions and contact information. The customers were instructed to examine your inventory and discontinue use of the kits immediately. Qualigen will send you replacement kits and provide you with a shipping label to return all of the defective kits including any that were partially used. Feel free to contact System Support at 760.579.6900 if you have any questions or require assistance with returning your kits.
Quantity in Commerce 17
Distribution US Distribution to states of: AL, CA, KS, KY, IN, MA, NC, NY, NV, OK, SC, TN, TX, UT, VA, and WA.
Total Product Life Cycle TPLC Device Report

1 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
510(K) Database 510(K)s with Product Code = CEC and Original Applicant = Qualigen, Inc.
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