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Recall Observatory FDA recall evidence

Device product

ANGIOGRAPHIC KIT W/MX123-3MR MANIFOLD, Model Number MX1030. for use during angiography and other special procedures.

Z-1475-2021

March 31, 2021

Class II

Product summary

Firm
Smiths Medical ASD Inc.
Event
Event 87647
Status
Terminated
Classification
Class II
Quantity
5540 devices
Official record key
device-enforcement:Z-1475-2021

Official wording

Reason: 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.

Code information: Lot Numbers: 3979813, 3982717, 4016454, 4024471

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.