Hill-Rom PRO+ 36" MRS Surface mattress, REF P7924A03.
Check against the official notice below — it lists the full affected range.
Baxter Healthcare Corporation is recalling 404 Hill-Rom PRO+ 36" MRS Surface mattresses (model REF P7924A03) distributed worldwide, including in multiple U.S. states and Canada. The mattresses have a failure mode that can reduce the performance of the Microclimate Management feature, which is designed to pull heat and moisture away from patients. This reduction in performance increases the risk that patients could develop pressure ulcers.
The affected mattresses can be identified by their UDI number 00887761977884 and specific serial numbers beginning with W225BP, W330BP, W333BP, W334BP, W337BP, or W341BP. The recall source does not specify what remedy is available to affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in an increased patient risk of pressure ulcer development.
Reason for recall: The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in an increased patient risk of pressure ulcer development. Distribution: Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, CT, GA, IA, IN, KY, LA, MD, MI, MN, MO, NC, NJ, NM, NM, NY, OH, OK, RI, SD, TN, TX, VT, and WI. There was government distribution but no military distribution. The country of Canada. Quantity: 404 mattresses Lot/code info: UDI 00887761977884; Serial numbers: W225BP4122, W225BP4148, W225BP4154, W225BP4155, W225BP4157, W225BP4158, W225BP4161, W225BP4162, W225BP4167, W225BP4170, W225BP4117, W225BP4124, W225BP4126, W225BP4127, W225BP4129, W225BP4130, W225BP4134, W225BP4138, W225BP4139, W225BP4140, W225BP4141, W225BP4142, W225BP4146, W225BP4152, W225BP4153, W225BP4156, W225BP4159, W225BP4164, W225BP4165, W225BP4166, W225BP4168, W225BP4169, W225BP4171, W225BP4172, W225BP4147, W225BP4118, W225BP4160, W225BP4119, W225BP4120, W225BP4123, W225BP4145, W334BP6515, W337BP6576, W337BP6580, W334BP6516, W337BP6584, W333BP6408, W333BP6410, W334BP6519, W337BP6581, W337BP6582, W337BP6585, W334BP6469, W334BP6485, W334BP6514, W337BP6567, W337BP6568, W337BP6569, W337BP6570, W337BP6571, W337BP6574, W337BP6575, W337BP6577, W337BP6579, W337BP6614, W337BP6615, W337BP6621, W337BP6630, W337BP6636, W337BP6641, W337BP6642, W337BP6643, W337BP6644, W337BP6645, W341BP6675, W341BP6676, W341BP6684, W341BP6646, W341BP6681, W341BP6683, W330BP6387, W334BP6477, W334BP6478, W334BP6481, W334BP6534, W334BP6535, W337BP6565, W337BP6566, W337BP6572, W337BP6573, W337BP6578, W337BP6622, W337BP6623, W337BP6624, W337BP6625, W337BP6626, W337BP6628, W337BP6629, W337BP6631, W337BP6632, W337BP6633, W337BP6634, W337BP6635, W337BP6637, W337BP6638, W341BP6648, W341BP6655, W341BP6658, W341BP6659, W341BP6660, W341BP6661, W341BP6678, W341BP6679, W341BP6687, W334BP6509, W334BP6512, W334BP6523, W334BP6524, W330BP6367, W330BP6382, W330BP6383, W330BP6385,
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.