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U.S. Department of Health and Human Services

Class 2 Device Recall VITROS 5600 Integrated System

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 Class 2 Device Recall VITROS 5600 Integrated Systemsee related information
Date Initiated by FirmApril 26, 2012
Date PostedJune 01, 2012
Recall Status1 Terminated 3 on July 05, 2018
Recall NumberZ-1699-2012
Recall Event ID 61790
510(K)NumberK081543 
Product Classification Analyzer, chemistry (photometric, discrete), for clinical use - Product Code JJE
ProductVITROS 5600 Integrated System Software Version 1.6 & Below Product Usage: For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products Slides, VITROS Chemistry Products MicroTip Reagents and VITROS Immunodiagnostic Products Reagents.
Code Information Product code: 6802413; Serial numbers: 56000118 - 56001498
Recalling Firm/
Manufacturer		 Ortho-Clinical Diagnostics
1000 Lee Road
Rochester NY 14606
For Additional Information ContactJoe Falvo
585-453-3452
Manufacturer Reason
for Recall		Ortho Clinical Diagnostics is recalling VITROS 5600 Integrated System Software Version 1.6 and below because of an anomaly that may inadvertently add a surfactant to a CurveTip position.
FDA Determined
Cause 2		Software design
ActionOrtho Clinical Diagnostics (OCD) sent an Urgent Product Correction Notification letter dated April 26, 2012, via FedEx overnight courier to US consignees with VITROS 5600 Systems. The letter identified the affected product, problem and actions to be taken. Foreign affiliates were informed by email on April 26, 2012 of the issue and instructed to notify their consignees of the issue and actions. OCD recommend customers to group all DAT assays into a single run as described in the letter, until the next Software Version 2.0 is installed on their VITROS 5600 System. Customers were instructed to complete and return the Confirmation of Receipt form. For questions contact Customer Technical Services at 1-800-421-3311
Quantity in Commerce1357 units
DistributionWorldwide Distribution - US (nationwide)
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 = JJE
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