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U.S. Department of Health and Human Services

Class 2 Device Recall Siemens ADVIA Centaur iPTH ReadyPack Assay

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 Class 2 Device Recall Siemens ADVIA Centaur iPTH ReadyPack Assaysee related information
Date Initiated by FirmMay 14, 2013
Date PostedJune 06, 2013
Recall Status1 Terminated 3 on March 05, 2015
Recall NumberZ-1513-2013
Recall Event ID 65224
510(K)NumberK121981 
Product Classification Radioimmunoassay, parathyroid hormone - Product Code CEW
ProductADVIA Centaur iPTH ReadyPack Assay 500 Tests; REF 10492369, 10493615, 1049361. For in vitro diagnostic use in the quantitative determination of intact parathyroid hormone (iPTH).
Code Information Reagent Lot Numbers: 056301 and 56302 Kit Lot Number/Exp. Date: REF 10492369- 500 Tests 61639301 09 Nov 2011 REF 1 0493615 - 500 Tests 63607301 09 Nov 2011 68004301 09 Nov 2011 70229301 09 Nov 2011 74126301 09Nov2011 REF 10493616-500 Tests 62645302 09 Nov 2011 66612302 09 Nov 2011 74129302 09 Nov 2011
FEI Number 1219913
Recalling Firm/
Manufacturer		 Siemens Healthcare Diagnostics, Inc
333 Coney St
East Walpole MA 02032-1516
For Additional Information Contact
508-668-5000
Manufacturer Reason
for Recall		iPTH Assay- reagent and calibrator lots may have demonstrated higher than anticipated variability
FDA Determined
Cause 2		No Marketing Application
ActionSiemens sent an Urgent Medical Device Correction letter dated May 2013 to all affected customers. The letter identified the product, problem, and actions to be taken by the customers. For questions, contact your Siemens Technical Solutions Center or your local Siemens technical support.
Quantity in Commerce3302 Kits (500 test)
DistributionNationwide Distribution.
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 = CEW
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