Baxter Healthcare Corporation recalls PRO+ 40" MRS SURFACE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and
Baxter Healthcare recalls PRO+ 40" MRS SURFACE mattresses with AMT technology due to UDI label errors that may cause incorrect bed frame selection. Affected units have specific serial numbers and model numbers.
Lower-risk recall
There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product specifications and may lead to incorrect product identification or selection, potentially resulting in use with an incompatible bed frame.
What happened, in plain English
Baxter Healthcare is recalling PRO+ 40" MRS SURFACE mattresses with Advanced Microclimate Technology (AMT) because their Unique Device Identification (UDI) labels have errors. These errors could lead to using the mattress with an incompatible bed frame, which might cause improper function. Read more at govinfonow.com/recall/1292598-baxter-healthcare-pro-40-mrs-surface-mattress-recall-incorrect-labeling.
Source Summary by GovInfoNow · govinfonow.com/recall/1292598-baxter-healthcare-pro-40-mrs-surface-mattress-recall-incorrect-labeling · Published October 6, 2026 · Updated October 6, 2026 · FDA enforcement record: FDA #Z-3264-2026
Cite this page
“Baxter Healthcare PRO+ 40" MRS SURFACE Mattress Recall: Incorrect Labeling Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/1292598-baxter-healthcare-pro-40-mrs-surface-mattress-recall-incorrect-labeling. Based on FDA recall #Z-3264-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3264-2026%22&limit=1).
Why it’s dangerous
The UDI labels on these mattresses have errors that don't match the approved product specifications. This could cause incorrect identification of the mattress, leading to selection of an incompatible bed frame. Using an incompatible bed frame might result in improper function of the mattress.
Who’s affected
Patients using Baxter's PRO+ 40" MRS SURFACE mattresses with AMT technology are likely affected. Those who have the specific model and serial numbers listed in the recall are at risk of using the mattress with an incompatible bed frame.
How to tell if you have this one
Check for the model number P7924A14 and serial numbers A305BP8842 to A305BP8847 on the UDI label. The mattress uses a non-powered system for pressure redistribution and has Advanced Microclimate Technology (AMT).
- Brand
Baxter Healthcare- Category
Medical device
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
Worldwide distribution - US Nationwide and the country of Canada.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-3262-2026 | PRO+ MRS SURFACE FOR VERSACARE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and output valves to provide weight-based pressure redistribution whenever a patient moves or is repositioned, Model/Catalog Number: P3255A08; Serial Number: A171BP3769 - B057BP6765 UDI-DI Number: 00887761007543 | 169 units |
| Z-3263-2026 | PRO+ 36" MRS SURFACE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and output valves to provide weight-based pressure redistribution whenever a patient moves or is repositioned, Model/Catalog Number: P7924A13; Serial Number: A136BP2433 - B052BP6510 UDI-DI Number: 00887761007659 | 824 units |
| Z-3264-2026 | PRO+ 40" MRS SURFACE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and output valves to provide weight-based pressure redistribution whenever a patient moves or is repositioned, Model/Catalog Number: P7924A14; Serial Number: A305BP8842 - A305BP8847 UDI-DI Number: 00887761007666 | 6 units |
What to do — step by step
Check UDI Label
Look for the model number P7924A14 and serial numbers A305BP8842 to A305BP8847 on the UDI label.
Questions people ask
Why is this mattress being recalled?
The UDI label has errors that don't match approved product specifications, which could lead to incorrect bed frame selection.
What is the model number for this mattress?
The model number is P7924A14.
What serial numbers are affected?
Serial numbers A305BP8842 to A305BP8847 are affected.
Contact Baxter Healthcare
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-3264-2026 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-3264-2026 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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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-3264-2026 (August 18, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3264-2026 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.