Class 2 Device Recall UniCel DxC Synchron Clinical Systems and UniCel DxC Synchron Access Integrated Clinical Systems

• Date Initiated by Firm: April 22, 2014
• Date Posted: July 22, 2016
• Recall Status: Terminated on February 09, 2017
• Recall Number: Z-2272-2016
• Recall Event ID: 74569
• 510(K)Number: K042291 K060256 K103842
• Product Classification: Analyzer, chemistry (photometric, discrete), for clinical use - Product Code JJE
• Product: UniCel DxC Synchron Clinical Systems and UniCel DxC Synchron Access Integrated Clinical Systems; ; The affected part is Part number 70300. Part number 970300 is used to transfer No Foam Solution from the No Foam Bottle to the Waste B canister and the Waste Manifold on the DxC Hydro System. ; ; Catalog No.; UniCel DxC 800 Synchron Clinical Systems; UniCel DxC 600 Synchron Clinical Systems; UniCel DxC 600i Synchron Access Integrated Clinical Systems; UniCel DxC 880i Synchron Access Integrated Clinical Systems; UniCel DxC 660i Synchron Access Integrated Clinical Systems; ; Product Labeling Reference No. A93719; ; For the in vitro determination of a variety of general chemistries, therapeutic drugs, and other chemistries.
• Code Information: Up to and including 6133
• Recalling Firm/ Manufacturer: Beckman Coulter Inc.; 250 S Kraemer Blvd; Brea CA 92821-6232
• Manufacturer Reason for Recall: Possible leaking of No Foam solution from the No Foam Bottle Assembly on the UniCel DxC Synchron Systems.
• FDA Determined Cause: Nonconforming Material/Component
• Action: An Important Product Notice dated 4/22/14 was sent to all their customers to inform them that Beckman Coulter has identified a manufacturing issue with a plastic fitting on the No Foam Bottle Assembly which may crack and cause No Foam solution to leak. The letter informs the customers of the impact, action to be taken, and resolution. Customers are asked to inspect the No Foam Bottle Assembly for leaks prior to refilling the bottle. If leaks occur, customers should contact Customer Support Center following the instructions provided. Customers are instructed to complete the enclosed response form within 10 days. Customers with questions are instructed to contact the firm's Customer Support Center - Via our website, http://www.beckmancoulter.com/customersupport/support - Via phone, call 1-800-854-3633 in the United States and Canada - Outside the United States and Canada, contact your local Beckman Coulter Representative.
• Quantity in Commerce: 3,540 units total (1,067 units in US)
• Distribution: Worldwide Distribution -- United Arab Emirates, Angola, Australia, Belgium, Bulgaria, Canada, Switzerland, China, Colombia, Costa Rica , Czech Republic, Germany, Denmark, Egypt, Eritrea, Spain, Finland, France, United Kingdom, Greece, Guatemala, Hong Kong, Indonesia, Ireland, India, Italy, Jordan, Japan, Korea, Republic of, Kuwait, Lebanon, Lithuania, Morocco, Mexico, Malaysia, Namibia, Netherlands, Norway, New Zealand, Oman, Panama, Philippines, Pakistan, Poland, Portugal, Paraguay, Qatar, Romania, Serbia, Russian Federation, Rwanda, Saudi Arabia, Sweden, Singapore, Slovakia, Swaziland, Thailand, Tunisia, Turkey, Taiwan, US (including Puerto Rico), Vietnam, South Africa, and Zimbabwe.
• Total Product Life Cycle: TPLC 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) Database: 510(K)s with Product Code = JJE and Original Applicant = BECKMAN COULTER, INC.