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Teleflex Medical Europe Ltd recalls Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50 Product Usage: for use in resp
Recalled April 25, 2018 · FDA recall Z-1403-2018 · Teleflex Medical Europe
Hazard
These one-way valves may disconnect at the joint between the two components that make up the device, which would cause an interruption of ventilation to the patient. · FDA Class II
Units
103910 units
Sold at
US Nationwide in the states of AU, CA, NZ
Description
These one-way valves may disconnect at the joint between the two components that make up the device, which would cause an interruption of ventilation to the patient.
Product
Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50 Product Usage: for use in respiratory and anesthesia circuits to connect two or more components of a breathing system.
Manufacturer(s)
Teleflex Medical Europe Ltd
Made in
Ireland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →