Z-2581-2023 Class II Ongoing
FDA device recall Z-2581-2023 was initiated by Baxter Healthcare Corporation on August 10, 2023 and is designated Class II. Reason for recall: Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display. The recall status is ongoing. Affected quantity: 2 units.
Recall Details
- Product Type
- Devices
- Report Date
- September 20, 2023
- Initiation Date
- August 10, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2 units
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.
Distribution Pattern
US Nationwide distribution in the state of CA.
Code Information
Product Code: 75MT-B; UDI: 00732094209372; Serial Numbers: 100027582923 and 100027862923