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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 Progressa Bed Surfaces Recalled for Mattress Air Bladder Displacement

Agency Publication Date: March 26, 2025
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Summary

Baxter Healthcare Corporation is recalling approximately 2,126 units of Progressa Bed Surfaces because the internal air bladders inside the mattress may move out of their intended position. This displacement usually occurs when the head of the bed is elevated, which can cause a visible dip or sinkhole in the mattress surface. These beds are designed to treat or prevent complications for patients who cannot move, and a lack of proper support could impact patient care. No injuries have been reported to date, and the manufacturer initiated this recall voluntarily.

Risk

The shifting of air bladders causes a depression in the mattress that removes support from the patient. This defect could lead to patient discomfort, improper positioning, or skin integrity issues if the surface fails to provide the necessary pressure management or therapeutic support.

What You Should Do

  1. This recall affects Baxter Progressa Bed Surfaces used for treating immobility complications, specifically Product Codes P7520A19, P7520A20S, P7520A21, P7520A22S, P7520A23, P7520A24S, P7520A3, P7520A31, P7520A37, P7520A39, P7520A45, and P7520A4S.
  2. Identify your equipment by locating the Product Code and the Serial Number on the device label. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled bed surface if it is included in the affected list.
  4. Contact Baxter Healthcare Corporation or your authorized medical distributor immediately to arrange for the return, replacement, or correction of the device.
  5. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding medical device safety.

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: Progressa Bed Surfaces
Model / REF:
P7520A19
P7520A20S
P7520A21
P7520A22S
P7520A23
P7520A24S
P7520A3
P7520A31
P7520A37
P7520A39
P7520A45
P7520A4S
Serial Numbers (2422):
A008MW1489
Y298MW1411
Y298MW1412
Y298MW1413
Y298MW1414
Y298MW1415
Y298MW1416
Y298MW1417
Y298MW1418
Y298MW1419
Y298MW1420
Y298MW1421
Y298MW1452
Y298MW1453
Y298MW1454
Y298MW1455
Y298MW1456
Y298MW1457
Y298MW1458
Y298MW1459
Y298MW1460
Y298MW1461
Y298MW1463
Y298MW1464
Y298MW1465
Y298MW1466
Y298MW1467
Y298MW1468
Y298MW1469
Y298MW1470
Y298MW1471
Y298MW1472
Y298MW1473
Y298MW1474
Y298MW1475
Y298MW1580
Y298MW1581
Y298MW1582
Y298MW1583
Y298MW1584
Y298MW1585
Y298MW1586
Y298MW1587
Y298MW1588
Y298MW1589
Y298MW1590
Y298MW1591
Y298MW1592
Y298MW1593
Y298MW1594
UDI:
00887761999893
00887761999886
00887761999879
00887761999862
00887761999855
00887761999848
00887761999770
00887761999756
00887761999718
00887761999701
00887761999671
00887761999657

Intended to treat or prevent pulmonary or other complications associated with immobility.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96327
Status: Active
Manufacturer: Baxter Healthcare Corporation
Sold By: Baxter Healthcare Corporation; Authorized Medical Distributors
Manufactured In: United States
Units Affected: 2,126 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.