PlainRecalls
FDA Devices Moderate Class II Terminated

Tubing with male luer lock adapter (Component) a. 76 cm, REF 601280 b. 122 cm, REF 607281. component of extravascular blood-pressure Transducer.

Reported: April 28, 2021 Initiated: March 31, 2021 #Z-1480-2021

Product Description

Tubing with male luer lock adapter (Component) a. 76 cm, REF 601280 b. 122 cm, REF 607281. component of extravascular blood-pressure Transducer.

Reason for Recall

Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds, Stopcocks and Tubing and Medex LogiCal Kits may have been manufactured with insufficient or incomplete welds. These are components for various cardiac kits including pressure monitoring devices and interventional imaging devices.

Details

Recalling Firm
Smiths Medical ASD Inc.
Units Affected
11340 units
Distribution
Distribution US nationwide including Puerto Rico, Austria, Canada, Chile, Ecuador, Hong Kong, Mexico, Slovenia, Brazil, South Africa, Colombia, and Japan.
Location
Minneapolis, MN

Frequently Asked Questions

What product was recalled?
Tubing with male luer lock adapter (Component) a. 76 cm, REF 601280 b. 122 cm, REF 607281. component of extravascular blood-pressure Transducer.. Recalled by Smiths Medical ASD Inc.. Units affected: 11340 units.
Why was this product recalled?
Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds, Stopcocks and Tubing and Medex LogiCal Kits may have been manufactured with insufficient or incomplete welds. These are components for various cardiac kits including pressure monitoring devices and interventional imaging devices.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 28, 2021. Severity: Moderate. Recall number: Z-1480-2021.