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U.S. Department of Health and Human Services

Class 2 Device Recall Perfusion Tubing Set

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 Class 2 Recall
Perfusion Tubing Set
see related information
Date Posted November 15, 2010
Recall Status1 Terminated on December 17, 2010
Recall Number Z-0374-2011
Recall Event ID 57052
Premarket Notification
510(K) Number
Product Classification Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass - Product Code DWF
Product Sorin OptiPack, Perfusion Tubing Set, Sterile EO, REF 084500201, Manufactured by Sorin Group USA, Inc. 14401 W. 65th Way Arvada, CO 80004 Indicated for use in surgical procedures requiring extracorporeal support for periods of up to six hours.
Code Information Lot No. 1020100025
Recalling Firm/
Sorin Group USA, Inc.
14401 W 65th Way
Arvada, Colorado 80004
Manufacturer Reason
for Recall
Defective product packaging may compromise product sterility.
Action Sorin Group sent an "URGENT: FIELD SAFETY NOTICE" letter dated October 7, 2010, to all customers. The letter described the product, problem and action to be taken by customer. The customers were instructed to check all affected inventory to exam for holes. Any damaged products were to be returned to Sorin. If no damage was found, product could be used. The customers were also instructed to contact Sorin Cardiopulmonary Customer Service at 1-800-650-2623 to return product and receive replacement; they were to share this information with all personnel who may use this product; and to complete and return the attached Customer Response Form via the self-addressed prepaid envelope provided or fax to (303) 467-6502 as soon as possible. For further information, contact 1-800-650-2623.
Quantity in Commerce 10
Distribution Nationwide distribution: CA, FL, IL, IN, KS, MD, MO, NE, NJ, NM, TN, TX, and VA.
Total Product Life Cycle TPLC Device Report

1 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 = DWF and Original Applicant = COBE LABORATORIES, INC.