Baxter Healthcare Corporation: Device Recall

Recall #Z-1816-2025 · 05/06/2025

Class II: Risk

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.

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.