Baxter PRO+ 36-inch Mattress Recalled for UDI Labeling Error
Baxter Healthcare is recalling 824 PRO+ 36-inch MRS Surface mattresses due to errors in the Unique Device Identification (UDI) label. The discrepancies may lead to incorrect product identification or use with incompatible bed frames.
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, which typically corresponds to a moderate severity score. The hazard involves labeling errors that may lead to incorrect product selection or use with incompatible equipment, but no specific injuries or illnesses are reported in the source text.
Plain-English summary
Baxter Healthcare Corporation is recalling 824 units of the PRO+ 36" MRS SURFACE mattress, Model/Catalog Number P7924A13. This medical device uses a non-powered system of intake and output valves to provide weight-based pressure redistribution. The affected units were distributed worldwide, including the United States and Canada.
The recall was initiated because of 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 FDA notes that this error may lead to incorrect product identification or selection, potentially resulting in the mattress being used with an incompatible bed frame.
Healthcare facilities and consumers who possess this specific model should verify the serial numbers against the range A136BP2433 through B052BP6510 or the UDI-DI Number 00887761007659. Users should contact Baxter Healthcare Corporation for instructions on how to resolve the labeling issue and ensure the device is compatible with their existing bed frames.
The recalled product
- Product
- 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
- Manufacturer
- Baxter Healthcare Corporation
- Affected units
- 824
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: A136BP2433 - B052BP6510 UDI-DI Number: 00887761007659
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+ 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
- 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
- HighBecton, Dickinson ForeSight Elite Tissue Oximetry Cable Recall for Incorrect Channel Switching
FDA (Devices) · 2026-09-30