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Merit Medical Systems, Inc. recalls Pressure Monitoring Tubing, PM6006. Pressure Monitoring Tubing (PM series) is used between the manifold and transducer
Recalled April 9, 2014 · FDA recall Z-1319-2014 · Merit Medical Systems
Hazard
The products are labeled as sterile but were not sterilized. · FDA Class II
Units
80
Sold at
Worldwide Distribution - USA Nationwide in the state of WI and countries of Thailand and Hong Kong.
Description
The products are labeled as sterile but were not sterilized.
Product
Pressure 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.
Manufacturer(s)
Merit Medical Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →