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U.S. Department of Health and Human Services

Class 2 Device Recall Terumo Cardiovacular

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 Class 2 Device Recall Terumo Cardiovacularsee related information
Date Initiated by FirmJune 04, 2013
Date PostedDecember 27, 2013
Recall Status1 Terminated 3 on October 01, 2014
Recall NumberZ-0603-2014
Recall Event ID 67064
510(K)NumberK820297 
Product Classification Valve, pressure relief, cardiopulmonary by Medical - Product Code MNJ
ProductTerumo Cardiovascular Custom Cardiovascular Procedure Kits containing an Overpressure Safety Valve, LN130B, in the Arterial Recirculation Line
Code Information N/A
Recalling Firm/
Manufacturer		 Terumo Cardiovascular Systems Corporation
125 Blue Ball Rd
Elkton MD 21921-5315
For Additional Information Contact
410-392-7102
Manufacturer Reason
for Recall		Over-Pressure Safety Valves not cleared with an indication for use on the arterial side of the extracorporeal bypass circuit.
FDA Determined
Cause 2		Component design/selection
ActionTerumo Cardiovascular issued Customer notification letters on June 4, 2013. Accounts advised to: Review this notice and decide to continue to use or not use the Cardiovascular Procedure Kits as configured until a replacement kit with a one-way valve indicated for use on the arterial side of the perfusion circuit is available. If you have questions, contact Terumo CVS Customer Service: 800-521-2818.
Quantity in Commerce24,227.
DistributionNationwide Canada
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 = MNJ
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