PlainRecalls
FDA Devices Moderate Class II Ongoing

Welch Allyn Connex Spot Monitor

Reported: September 20, 2023 Initiated: August 10, 2023 #Z-2581-2023

Product Description

Welch Allyn Connex Spot Monitor

Reason for Recall

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

Details

Units Affected
2 units
Distribution
US Nationwide distribution in the state of CA.
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
Welch Allyn Connex Spot Monitor. Recalled by Baxter Healthcare Corporation. Units affected: 2 units.
Why was this product recalled?
Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 20, 2023. Severity: Moderate. Recall number: Z-2581-2023.