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U.S. Department of Health and Human Services

Class 2 Device Recall FastPack Total PSA Immunoassay

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 Class 2 Device Recall FastPack Total PSA Immunoassaysee related information
Date Initiated by FirmNovember 08, 2013
Date PostedDecember 19, 2013
Recall Status1 Terminated 3 on September 18, 2014
Recall NumberZ-0547-2014
Recall Event ID 66842
510(K)NumberK994419 
Product Classification Prostate-specific antigen (psa) for management of prostate cancers - Product Code LTJ
ProductFastPack Total PSA Immunoassay Chemilunescence assay for the determination of Total PSA. FastPack Total PSA Immunoassay is a paramagnetic particle immunoassay for the in vitro quantitative determination of prostate-specific antigen (PSA) in human serum and plasma as an aid in the management of patients with prostate cancer. The FastPack Total PSA Immunoassay is designed for use with the FastPack System.
Code Information Total PSA: Catalog Number 25000040. Lot Number 1309038-10P Exp Date 6/26/2013.
FEI Number 3003355251
Recalling Firm/
Manufacturer		 Qualigen Inc
2042 Corte del Nogal
Carlsbad CA 92011-1438
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
ActionQualigen, 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 Commerce182
DistributionUS Distribution to states of: AL, CA, KS, KY, IN, MA, NC, NY, NV, OK, SC, TN, TX, UT, VA, and WA.
Total Product Life CycleTPLC Device Report
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.
510(K) Database510(K)s with Product Code = LTJ
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