Welch Allyn Connex Spot Monitor — FDA record Z-2581-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Aug 10, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Welch Allyn Connex Spot Monitor
Reason
Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display.
Classification
Class II
Recalling firm
Baxter Healthcare Corporation
Quantity
2 units
Agency-reported status
Ongoing
Source record identifier
Z-2581-2023

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityProduct Code: 75MT-B; UDI: 00732094209372; Serial Numbers: 100027582923 and 100027862923

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide distribution in the state of CA.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Sep 20, 2023
Recall initiation date
Aug 10, 2023
Center classification date
Sep 12, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

Related records