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Recall Observatory FDA recall evidence

Device product

Welch Allyn Connex Spot Monitor

Z-2581-2023

August 10, 2023

Class II

Product summary

Firm
Baxter Healthcare Corporation
Event
Event 92874
Status
Ongoing
Classification
Class II
Quantity
2 units
Official record key
device-enforcement:Z-2581-2023

Official wording

Reason: Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display.

Code information: Product Code: 75MT-B; UDI: 00732094209372; Serial Numbers: 100027582923 and 100027862923

Distribution pattern: US Nationwide distribution in the state of CA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display.