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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices

Baxter Affinity 4 Birthing Beds Recalled for Risk of Bed Movement Failure

Agency Publication Date: May 23, 2025
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Summary

Baxter Healthcare Corporation is recalling 164 Affinity 4 Birthing Beds because a defect in the wiring for the bed's motors (actuators) may prevent the bed or its foot section from being lowered. This mechanical failure is caused by improper crimps on the signal wires. While no injuries have been reported, a bed that cannot be adjusted properly can interfere with patient care during delivery. The recall covers 28 different product codes and specific serial numbers manufactured in the United States.

Risk

The improper wiring crimps can cause the bed's movement to fail, specifically preventing the bed or foot section from lowering. This failure could cause positioning delays or patient discomfort during medical procedures.

What You Should Do

  1. This recall involves Affinity 4 Birthing Beds with various product codes including P3700E100429, P3700E100432, P3700E100433, and several others.
  2. Identify if your equipment is affected by checking the product code and serial number located on the device label. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device.
  4. Contact Baxter Healthcare Corporation or your distributor to arrange return, replacement, or correction.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional questions.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Affinity 4 Birthing Bed
Model / REF:
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
P3700E100477
Serial Numbers (164):
A008AA9216
A008AA9217
A009AA9218
A009AA9219
A009AA9220
A031AA9361
A031AA9362
A042AA9428
Z352AA9154
Z352AA9155
Z353AA9169
Z354AA9172
Z354AA9173
Z354AA9175
Z354AA9177
A014AA9267
A008AA9214
A015AA9274
A015AA9285
A016AA9286
A016AA9287
Z358AA9187
Z345AA9079
Z345AA9080
Z345AA9081
Z346AA9088
Z346AA9089
Z346AA9090
Z346AA9091
Z346AA9098
Z347AA9112
Z348AA9120
Z348AA9121
Z348AA9122
Z348AA9123
Z348AA9124
Z348AA9125
A008AA9206
A009AA9222
A015AA9273
A034AA9371
A034AA9375
Z345AA9071
Z345AA9072
Z345AA9073
Z345AA9074
Z345AA9075
Z345AA9076
Z345AA9077
Z345AA9078
UDI:
00887761000896

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96779
Status: Active
Manufacturer: Baxter Healthcare Corporation
Sold By: Baxter Healthcare Corporation
Manufactured In: United States
Units Affected: 164 units
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.