Baxter Healthcare Corporation is recalling 232 Hill-Rom PRO+ 36-inch MRS Surfaces (mattresses) because inconsistencies were found in service records from a previous safety correction. The company needs to reassess these specific mattresses to ensure they were correctly repaired and that the correct serial numbers were documented. These mattresses are used for patient support and to help prevent or treat pressure injuries, and an incomplete repair could affect their performance.
If the previous safety corrections were not performed accurately due to record-keeping errors, the mattress may not function as intended, potentially failing to provide the necessary support or pressure relief for patients.
You have 2 options:
Reassessment and correction of impacted mattresses
Healthcare provider or manufacturer consultation
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.
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 · Raw API Response
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