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U.S. Department of Health and Human Services

Class 2 Device Recall Pressure Monitoring Tubing

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 Class 2 Device Recall Pressure Monitoring Tubingsee related information
Date Initiated by FirmMarch 13, 2014
Date PostedApril 03, 2014
Recall Status1 Terminated 3 on July 07, 2014
Recall NumberZ-1319-2014
Recall Event ID 67844
510(K)NumberK883718 
Product Classification Pressure Monitoring Tubing - Product Code OBI
ProductPressure Monitoring Tubing, PM6006. Pressure Monitoring Tubing (PM series) is used between the manifold and transducer as a conduit to transmit the fluid pressure of the patient to the pressure transducer.
Code Information Lot Number H591335
Recalling Firm/
Manufacturer		 Merit Medical Systems, Inc.
1600 West Merit Parkway
South Jordan UT 84095
For Additional Information ContactPaul Kennedy
801-208-4301
Manufacturer Reason
for Recall		The products are labeled as sterile but were not sterilized.
FDA Determined
Cause 2		Release of Material/Component prior to receiving test results
ActionMerit Medical sent an Urgent Product Recall Notice dated March 14, 2014 to all customers and sales representatives via email. The letter identified the affected product, problem and actions to be taken. Customers were provided a Product Retrieval Form, product identification information, instruction to immediately quarantine any devices and discontinue use, ensure all personnel to whom devices were distributed are made aware of this field action, and instructions to contact their Merit representative to arrange product return and replacement. For questions call 1-801-316-4822.
Quantity in Commerce80
DistributionWorldwide Distribution - USA Nationwide in the state of WI and countries of Thailand and Hong Kong.
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 = OBI
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