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U.S. Department of Health and Human Services

Class 2 Device Recall Haemonetics cardioPAT Cardiovascular Perioperative Autotransfusion System

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 Class 2 Device Recall Haemonetics cardioPAT Cardiovascular Perioperative Autotransfusion Systemsee related information
Date Initiated by FirmJuly 27, 2011
Date PostedAugust 05, 2011
Recall Status1 Terminated 3 on June 09, 2014
Recall NumberZ-2956-2011
Recall Event ID 59379
510(K)NumberK053000 
Product Classification Apparatus, autotransfusion - Product Code CAC
ProductHaemonetics cardioPAT -Cardiovascular Perioperative Autotransfusion System Model 2050 US Models Out-Side the US: 02050-UK, 02050-ES, 02050-IT, 02050-NL, 02050-GE, 02050-FR, 02050-JA The Haemonetics Cardiovascular Perioperative Autotransfusion System for Use (cardioPAT) is indicated for use to salvage red blood cells from blood lost intraoperatively and postoperatively during cardiovascular surgical procedures, where the expected rate of processing of salvaged blood and fluid aspirated from the surgical site is less than or equal to two liters per hour.
Code Information All serial numbers
FEI Number 1219343
Recalling Firm/
Manufacturer		 Haemonetics Corporation
400 Wood Rd
Braintree MA 02184-2412
For Additional Information ContactSAME
781-848-7100
Manufacturer Reason
for Recall		Updated Operations Manual for the deployment of the spill collection system and cleaning
FDA Determined
Cause 2		Component design/selection
ActionHaemonetics sent a "FIELD NOTIFICATION: UPDATE OF CardioPAT OPERATIONS MANUAL FOR DEPLOYMENT OF SPILL COLLECTION BAG AND CLEANING" letter dated July 27, 2011 to all affected customers. The letter describes the product, problem, and the actions to be taken by the customers. The letter requests that customers complete an enclosed Customer Confirmation sheet indicating that the affected devices are in their possession and to return the sheet via fax to Haemonetics at 781-987-9252. Additionally, instructions for deployment of the spill collection drainage system, revised Operations Manual and Quick Reference Guide Addendum are enclosed with the letter. Contact Haemonetics at 1-800-537-2802 for questions regarding this notice..
Quantity in Commerce316 units
DistributionWorldwide Distribution--USA (nationwide) and the countries of Canada, France, Germany, Great Britain, Italy, Japan, Spain, and The Netherlands.
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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