Z-1473-2021 Class II Terminated

Recalled by Smiths Medical ASD Inc. — Minneapolis, MN

FDA device recall Z-1473-2021 was initiated by Smiths Medical ASD Inc. on March 31, 2021 and is designated Class II. 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 f… The recall status is terminated (terminated March 20, 2023). Affected quantity: 3740 devices.

Recall Details

Product Type
Devices
Report Date
April 28, 2021
Initiation Date
March 31, 2021
Termination Date
March 20, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
3740 devices

Product Description

LogiCal Left Heart Kit, Model Number M20553. for blood pressure monitoring.

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.

Distribution Pattern

Distribution US nationwide including Puerto Rico, Austria, Canada, Chile, Ecuador, Hong Kong, Mexico, Slovenia, Brazil, South Africa, Colombia, and Japan.

Code Information

Lot Numbers: 3995542, 4002489, 4016473, 4048833,4069387