Date Initiated by Firm | November 08, 2013 |
Date Posted | December 04, 2013 |
Recall Status1 |
Terminated 3 on May 27, 2014 |
Recall Number | Z-0450-2014 |
Recall Event ID |
66759 |
510(K)Number | K944320 |
Product Classification |
Set, administration, intravascular - Product Code FPA
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Product | SmartSite Low Sorbing Infusion Set with Texium Close Male Luer, Model No. 24301-0007T
The SmartSite Low Sorbing Infusion Sets with Texium Male Luer are used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein. |
Code Information |
Lot No: 13046215 13046641 13056285 13056577 13075931 |
Recalling Firm/ Manufacturer |
CareFusion 303, Inc. 10020 Pacific Mesa Blvd San Diego CA 92121-4386
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For Additional Information Contact | 858-617-4000 |
Manufacturer Reason for Recall | CareFusion is recalling the SmartSite Low Sorbing Infusion Set with Texium Closed Male Luer because it is not assembled with low-sorbing tubing. |
FDA Determined Cause 2 | Employee error |
Action | The firm, CareFusion, sent an "URGENT: Medical Device Recall Notification" letter dated November 8, 2013 to all customers who purchased the SmartSite Low Sorbing Infusion Set with Texium Closed Male Luer. The letter informs the customers of the problems identified and the actions to be taken. Customers are instructed to immediately complete and return to CareFusion the enclosed, pre-addressed and postage paid, Recall Response Card and return all recalled product directly to the distributor form whom it was purchased. Customers with questions are instructed to contact their distributor directly or call the CareFusion Support Center at (888) 562-6018.
If you have recall related questions or need support, please call CareFusion Support Center at 1-888-562-6018; hours: 7am to 4pm PST or Technical Support at 1-888-812-3229; hours 7am to 5pm PST. |
Quantity in Commerce | 480 units |
Distribution | US Distribution in CA, WY, OH, UT, and MA. |
Total Product Life Cycle | TPLC Device Report |
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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.
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510(K) Database | 510(K)s with Product Code = FPA
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