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Class 2 Device Recall Thermal dot matrix printer |
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Date Initiated by Firm |
November 07, 2005 |
Date Posted |
January 06, 2006 |
Recall Status1 |
Terminated 3 on March 14, 2006 |
Recall Number |
Z-0348-06 |
Recall Event ID |
34082 |
510(K)Number |
K993341
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Product Classification |
Syringe, Balloon Inflation - Product Code MAV
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Product |
IntelliSystem II Thermal Dot Matrix printer 110 V adapter and fiber optic serial interface 10m cable |
Code Information |
Catalog Number IN1600. Serial Numbers: T2370-0004, T2370-0007, T2370-0013, T2370-0014, T2370-0018, T2370-0019, T2370-0021, T2370-0023, T2370-0029, T2370-0030, T2370-0031, T2370-0032, T2370-0034, T2370-0041, T2370-0043, T2370-0044, T2370-0045, T2370-0047, T2370-0048, T2370-0049, T2370-0050, T2370-0059, T2370-0063, T2370-0064, T2370-0074, T2482-0029 |
Recalling Firm/ Manufacturer |
Merit Medical Systems, Inc 1600 West Merit Pkwy South Jordan UT 84095-2416
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For Additional Information Contact |
801-208-4405
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Manufacturer Reason for Recall |
Dot matrix printer, as a component of a pressure monitoring system, may overheat and pose a fire hazard.
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FDA Determined Cause 2 |
Other |
Action |
Sale representatives and consignees were notified by letter. |
Quantity in Commerce |
26 units |
Distribution |
Device was distributed in the US, Canada and worlwide. US distribution includes: AL, IN, MD, MS, NJ, OH, OR, PA, TN, TX, and WA. Foreign consignees include: Argentinal, Australia, Belgium, Brazil, France, Germany, Israel, Japan, Mexico, Netherland, New Zealand, UK and Wales. |
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 = MAV and Original Applicant = MERIT MEDICAL SYSTEMS, INC.
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