Baxter Healthcare Corporation: Device Recall
Recall #Z-1563-2025 · 03/21/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1563-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Baxter Healthcare Corporation
- Status
- Ongoing
- Date Initiated
- 03/21/2025
- Location
- Deerfield, IL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 70627 units
Reason for Recall
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Product Description
Welch Allyn Welch Allyn Connex Spot Monitor, Product Code/ Part Numbers: 1) 73WT-B; 2) 74CE-B; 3) 74CT-B; 4) 74CX-B; 5) 74ME-B; 6) 74MT-B; 7) 74MX-B; 8) 74RE-B; 9) 74RT-B; 10) 75CE-B; 11) 75CT-B; 12) 75CT-BR; 13) 75CX-B; 14) 75-HCA-CTB; 15) 75-HCA-MTB; 16) 75ME-B; 17) 75MT-B; 18) 75MT-BR; 19) 75MX-B; 20) 75RE-B; 21) 75RT-B; 22) 75WE-B; 23) 75WT-B.
Distribution Pattern
Worldwide distribution.
Other Recalls by Baxter Healthcare Corporation
- Class II: Risk 12/22/2025
- Class II: Risk 11/28/2025
- Class II: Risk 10/28/2025
- Class II: Risk 09/17/2025
- Class II: Risk 08/29/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.