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U.S. Department of Health and Human Services

Class 2 Device Recall Atrium Medical Express Dry Seal ATS

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 Class 2 Device Recall Atrium Medical Express Dry Seal ATSsee related information
Date Initiated by FirmNovember 19, 2013
Date PostedJanuary 14, 2014
Recall Status1 Terminated 3 on June 11, 2015
Recall NumberZ-0743-2014
Recall Event ID 66788
510(K)NumberK043140 K043582 
Product Classification Apparatus, autotransfusion - Product Code CAC
ProductAtrium Express Dry Seal ATS (Autotransfusion) Blood Recovery System Chest Drain with Prefilled Air Leak Monitor; Product Code: 4050-100P. To evacuate air and/or fluid from the chest cavity or mediastinum.
Code Information Lot number starting with 10883097 and the ending lot number 10913346 (All units in between and including these two numbers)
Recalling Firm/
Manufacturer		 Atrium Medical Corporation
5 Wentworth Dr
Hudson NH 03051-4929
For Additional Information ContactKenneth Collins
603-880-1433
Manufacturer Reason
for Recall		Chest Drain tubing of of the ATS Blood recovery may leak or disconnect
FDA Determined
Cause 2		Device Design
ActionAtrium Medical issued notification letters to direct consignees by UPS next day on 19 November 2013, and indirect consignees (distributors customers) by UPS next day or USPS priority (for customers with a PO Box) on 27 November 2013. The Letter explain the issue and the steps that should be taken. The customer will be offered replacement with unaffected product or credit. The firm describes Procedures for Emergency Use. The firm identifies potential product substitutions. These products are the same drainage product without the auto-transfusion line. International Distributors. International distributors provided with the Recall Authorization' package and the customer letter. Accounts are requested to complete the Recall Reply Form acknowledging receipt of the notification. Contact Atrium Medical Customer Service at 1-800-370-7899, Monday through Friday between 9:00 am to 5:00 pm.
Quantity in Commerce1,944 units
DistributionWorldwide Distribution-USA (nationwide) and the countries of Australia, Canada, Austria, Ireland, Romania, South Africa, Colombia, Lebanon Netherlands, Jordan, Russia, and Taiwan.
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 = CAC
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