Z-2581-2023 Class II Ongoing
FDA device recall Z-2581-2023 was initiated by Baxter Healthcare Corporation on Aug 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
- Sep 20, 2023
- Initiation Date
- Aug 10, 2023
- 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
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2581-2023
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026