Baxter Healthcare Corporation Welch Allyn Connex Spot Monitor Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Welch Allyn Connex Spot Monitor
Brand
Baxter Healthcare Corporation
Lot Codes / Batch Numbers
Product Code: 75MT-B, UDI: 00732094209372, Serial Numbers: 100027582923 and 100027862923
Products Sold
Product Code: 75MT-B; UDI: 00732094209372; Serial Numbers: 100027582923 and 100027862923
Baxter Healthcare Corporation is recalling Welch Allyn Connex Spot Monitor due to Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display.
Recommended Action
Per FDA guidance
The consignee recall notification was sent out via email 08/10/2023. The letter instructs the consignee to immediately locate, isolate, and cease all use of the affected product, contact Baxter Customer Service and Technical Support to arrange for return and replacement of the impacted units, acknowledge receipt by responding on the customer portal, and notify other affected customers of the consignee. Affected product will be removed from the field and customers will receive replacement units of the Connex Spot Monitor. Impacted product will be returned to Baxter and will be destroyed per the Return Material Authorization process.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026