Reported Apr 10, 2024 · Ongoing
Hill-Rom PRO+ 36" MRS Surface, REF P7924A03, The pro+ mattress is intended for patient support and for the prevention…
Baxter Healthcare Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
- Hill-Rom PRO+ 36" MRS Surface, REF P7924A03, The pro+ mattress is intended for patient support and for the prevention and/or treatment of pressure injuries.
- Lot codes and dates
- UDI/DI 00887761977884
- Serial Numbers
232 of 232 codes
W330BP6363W333BP6439W334BP6477W334BP6535W337BP6631W341BP6675X047BP7353X049BP7431W330BP6365W333BP6440W334BP6478W334BP6536W337BP6632W341BP6676X047BP7354X049BP7432W330BP6366W333BP6442W334BP6480W334BP6537W337BP6633W341BP6678X047BP7355X049BP7433W330BP6367W333BP6445W334BP6481W337BP6565W337BP6634W341BP6679X047BP7356X063BP7505W330BP6368W333BP6446W334BP6485W337BP6566W337BP6635W341BP6681X047BP7357X063BP7506W330BP6382W333BP6447W334BP6486W337BP6567W337BP6636W341BP6683X047BP7358X063BP7507W330BP6383W333BP6448W334BP6487W337BP6568W337BP6637W341BP6684X047BP7359X063BP7508W330BP6385W333BP6450W334BP6489W337BP6569
- Amount recalled
- 232 units
Where it was sold
- Nationwide
- CO
Why it was recalled
Inconsistencies were identified with service records associated with corrections performed for a previous Medical Device Correction issued by Baxter (ref number: FA-2022-026). Your devices have been identified as potentially impacted by these service inconsistencies and therefore, Baxter will need to reassess the impacted mattresses to confirm they have been corrected as identified by the service order, and to confirm the correct serial numbers have been identified.
This product could cause temporary or reversible health problems — stop using it.
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