FDA recall Z-2581-2023
Baxter Healthcare Corporation · Class II · device
Product
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.
Distribution
US Nationwide distribution in the state of CA.
Key facts
- Status
- Ongoing
- Initiation date
- 2023-08-10
- Report date
- 2023-09-20
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Deerfield, IL, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2581-2023