Baxter Healthcare Progressa Bed Surfaces Recall: Air Bladders May Move Out of Position
Baxter Healthcare recalls Progressa Bed Surfaces with product codes P7520A19 to P7520A4S. Air bladders may move out of position when the head of the bed is elevated, causing a dip in the mattress. Consumers should check if their unit has the listed serial numbers or product codes.
Use caution until it’s fixed
The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.
Contact the company
What happened, in plain English
Baxter Healthcare is recalling Progressa Bed Surfaces that may cause a dip in the mattress when the head of the bed is elevated. This happens because the air bladders inside the mattress can move out of position. If you own one of these models, you should check if it's affected and take action. Read more at govinfonow.com/recall/52769-baxter-healthcare-progressa-bed-surfaces-recall-air-bladders-may-move.
Source Summary by GovInfoNow · govinfonow.com/recall/52769-baxter-healthcare-progressa-bed-surfaces-recall-air-bladders-may-move · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1468-2025
Cite this page
“Baxter Healthcare Progressa Bed Surfaces Recall: Air Bladders May Move Out of Position.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52769-baxter-healthcare-progressa-bed-surfaces-recall-air-bladders-may-move. Based on FDA recall #Z-1468-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1468-2025%22&limit=1).
Why it’s dangerous
The air bladders inside the mattress can move out of position when the head of the bed is elevated. This causes a dip in the mattress, which may lead to discomfort or injury if the patient's body is not properly supported.
Who’s affected
People who own or use Progressa Bed Surfaces with the listed product codes or serial numbers are most at risk. This includes patients in hospitals or homes who use the bed for immobility treatment.
How to tell if you have this one
Check if your Progressa Bed Surface has product codes P7520A19, P7520A20S, P7520A21, P7520A22S, P7520A23, P7520A24S, P7520A3, P7520A31, P7520A37, P7520A39, P7520A45, or P7520A4S. Also check the serial numbers listed in the recall notice.
- Brand
Baxter Healthcare- Category
Medical device
What to do — step by step
Check Product Codes
Look for product codes P7520A19 through P7520A4S on your Progressa Bed Surface.
Check Serial Numbers
Verify if your unit has any of the listed serial numbers in the recall notice.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide. Global Distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 36 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-1468-2025 (February 25, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1468-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.