Baxter PRO+ Mattress Recalled for UDI Labeling Error
Baxter Healthcare is recalling six PRO+ 40-inch MRS Surface mattresses due to errors in the Unique Device Identification (UDI) label text.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves a labeling error that could lead to the use of an incompatible bed frame, fitting the criteria for moderate severity without reported injuries.
Plain-English summary
Baxter Healthcare Corporation is recalling six units of the PRO+ 40" MRS SURFACE mattress, Model/Catalog Number P7924A14. The recall is due to an error in the product description on the Unique Device Identification (UDI) label. These labeling discrepancies do not align with the approved product or product specifications.
The incorrect labeling may lead to incorrect product identification or selection, potentially resulting in the use of the mattress with an incompatible bed frame. The affected units were distributed worldwide, including the United States and Canada.
Healthcare facilities and users should identify the affected units by checking for Serial Numbers A305BP8842 through A305BP8847 or UDI-DI Number 00887761007666. Users should contact Baxter Healthcare Corporation for instructions on how to proceed with the recall.
The recalled product
- Product
- 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
- Manufacturer
- Baxter Healthcare Corporation
- Affected units
- 6
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Serial Number: A305BP8842 - A305BP8847 UDI-DI Number: 00887761007666
Distribution
Distributed nationwide across the United States.
Related recalls
Same manufacturer · Baxter Healthcare Corporation
See all →- ModerateBaxter Recalls PRO+ MRS Mattress Due to UDI Labeling Error
FDA (Devices) · 2026-09-30
- ModerateBaxter PRO+ 36-inch Mattress Recalled for UDI Labeling Error
FDA (Devices) · 2026-09-30
- ModerateBaxter Recalls Two VOLARA Systems Due to Potential Flow Rate Inaccuracy
FDA (Devices) · 2026-09-30
- SevereBaxter Recalls Dextrose Injection Bags Due to Stainless Steel Particulate Matter
FDA (Drugs) · 2026-09-16
- HighBaxter Recalls Clindamycin Injection Due to Manufacturing Deviations
FDA (Drugs) · 2026-09-09
Same hazard · mis labeling
See all →- ModerateVentec HomeFill Oxygen System Recalled for Missing Medical Gas Labeling
FDA (Devices) · 2026-09-30
- HighBecton, Dickinson ForeSight Elite Tissue Oximetry Cable Recall for Incorrect Channel Switching
FDA (Devices) · 2026-09-30
- HighWhole Foods Market Recalls Cabricharme Cheese for Undeclared Egg Allergen
FDA (Food) · 2026-09-30
- ModerateOlympus Endoscopic Balloon Dilator Recalled for Incorrect Inflation Chart Label
FDA (Devices) · 2026-09-30
- ModerateVentec HomeFill Oxygen System Recalled for Missing Medical Gas Labeling
FDA (Devices) · 2026-09-30