FDAClass IISeptember 20, 2023

Welch Allyn Connex Spot Monitor recall

Welch Allyn Connex Spot Monitor

Why was Welch Allyn Connex Spot Monitor recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
Welch Allyn Connex Spot Monitor
Recalling firm
Baxter Healthcare Corporation
Quantity
2 units
Distribution
US Nationwide distribution in the state of CA.
Recall date
September 20, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls