Baxter Healthcare recalls Affinity 4 Birthing Beds with specific product codes due to potential signal wire crimps causing loss of bed lowering function.
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.
Baxter Healthcare is recalling Affinity 4 Birthing Beds with certain product codes because improper crimps on signal wires might prevent the bed from lowering safely. This could lead to injury if the bed isn't properly adjusted during childbirth.
The signal wires connecting the bed's actuators can become improperly crimped, which may cause the bed to fail to lower properly. This could lead to unsafe positioning during childbirth if the bed doesn't adjust as needed.
Pregnant women and healthcare providers using the Affinity 4 Birthing Bed with the listed product codes and serial numbers. Those most at risk are individuals using the bed for childbirth deliveries.
Check the product code (P3700E100429 through P3700E100477) and serial number on the bed. The specific serial numbers listed in the recall notice are affected.
Ensure the bed can lower safely before using it again.
Reach out to Baxter Healthcare for assistance with the recall.
Product codes P3700E100429 through P3700E100477 with specific serial numbers listed in the recall notice.
Check the product code and serial number on your bed against the list of affected units provided in the recall notice.
Ensure the bed lowers safely before use and contact Baxter Healthcare for assistance.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1816-2025 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-1816-2025 from Baxter Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
