Baxter Healthcare Corporation: Device Recall
Recall #Z-1816-2025 · 05/06/2025
Recall Details
- Recall Number
- Z-1816-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Baxter Healthcare Corporation
- Status
- Ongoing
- Date Initiated
- 05/06/2025
- Location
- Deerfield, IL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 164 units
Reason for Recall
There is a potential for improper crimps on the signal wires of the actuators which could result in a loss of ability to lower the bed or the foot section of the bed.
Product Description
Affinity 4 Birthing Bed, Product Codes P3700E100429, P3700E100432, P3700E100433, P3700E100434, P3700E100435, P3700E100436, P3700E100437, P3700E100438, P3700E100439, P3700E100441, P3700E100442, P3700E100443, P3700E100444, P3700E100445, P3700E100446, P3700E100448, P3700E100449, P3700E100450, P3700E100453, P3700E100455, P3700E100456, P3700E100457, P3700E100459, P3700E100463, P3700E100468, P3700E100472, P3700E100476, and P3700E100477
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of BAHRAIN, Canada, Chile, FRANCE, KUWAIT, NETHERLANDS, NORWAY, UNITED ARAB EMIRATES.
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