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Class 2 Device Recall MOOG Curlin Infusion Administration Set |
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Date Initiated by Firm |
February 27, 2019 |
Date Posted |
July 23, 2019 |
Recall Status1 |
Terminated 3 on April 28, 2021 |
Recall Number |
Z-2053-2019 |
Recall Event ID |
82864 |
510(K)Number |
K981816
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Product Classification |
Pump, infusion - Product Code FRN
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Product |
MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carton, sterile. Product Usage: Administration set to be used with the Moog Curlin Infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.
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Code Information |
Lot numbers CF1819415, CF1820215, CF1821616, CF1822914, and CF1823615, UDI 38148440000464. |
Recalling Firm/ Manufacturer |
Zevex Incorporated (dba MOOG Medical Devices Group) 4314 S Zevex Park Ln Salt Lake City UT 84123-7881
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For Additional Information Contact |
Christopher Dodge 801-264-1001 Ext. 112
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Manufacturer Reason for Recall |
Administration sets leaked at the filter.
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FDA Determined Cause 2 |
Nonconforming Material/Component |
Action |
The recalling firm issued a letter dated 2/27/2019 via regular mail on 2/272019 to their direct accounts describing the issue, risk to health, and the necessary actions to be taken. |
Quantity in Commerce |
569/20-set caess |
Distribution |
Distribution was made to GA, IL, KS, MA, MI, and OH. There was no foreign/military/government distribution. |
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 = FRN and Original Applicant = BECTON DICKINSON CURLIN, LLC.
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