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U.S. Department of Health and Human Services

Class 2 Device Recall Haemonetics cardioPAT

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 Class 2 Device Recall Haemonetics cardioPATsee related information
Date Initiated by FirmJanuary 25, 2011
Date PostedFebruary 22, 2011
Recall Status1 Terminated 3 on January 14, 2013
Recall NumberZ-1391-2011
Recall Event ID 57805
510(K)NumberK053000 
Product Classification autotransfusion System - Product Code CAC
ProductHaemonetics cardioPAT Cardiovascular - autotransfusion System Catalog Number: 02050-US
Code Information All serial numbers
Recalling Firm/
Manufacturer		 Haemonetics Corporation
400 Wood Road
Braintree MA 02184-2412
For Additional Information Contact
781-848-7100
Manufacturer Reason
for Recall		Update Instructions for Use for the CardioPAT® Manual for Leak Detection. User may mis-interpret the air-leak rate displayed by the cardioPAT device when making a determination about chest-drain removal, which could result in the patient experiencing a pneumothorax.
FDA Determined
Cause 2		Labeling design
ActionHaemonetics issued a Field Correction Notice on 1/25/11 . with the Air Leak Detection addendum and index be inserted into the appropriate document, applied to all cardioPAT@ devices on site. The serial number for each cardioPAT device on site should be recorded on the attached acknowledgement and the completed acknowledgement should be returned to your Haemonetics Sales Consultant. A Haemonetics Sales Consultant will train on the content of these items and insert them into the Operator Manuals
Quantity in Commerce309 units
DistributionWorldwide distribution, including USA, Australia, Belgium, Canada, Switzerland, China, Germany, Finland, France, United Kingdom, Hong Kong, Israel, Italy, Japan, Netherlands, Russian Federation, and Sweden.
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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