Hill-Rom PRO+ MRS Surface For Versacare mattress, REF P3255A02.
Check against the official notice below — it lists the full affected range.
Baxter Healthcare Corporation is recalling Hill-Rom PRO+ MRS Surface mattresses (model reference P3255A02) for the Versacare mattress system. A failure in the affected mattresses 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 of pressure ulcer development in patients using these mattresses. The recall affects 202 mattresses that were distributed worldwide, including across numerous U.S. states and Canada, with specific serial numbers identified in the recall notice.
The recall includes specific serial numbers that customers should check against their equipment. The source document does not specify a remedy or instructions for what affected consumers should do regarding this recall.
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: 202 mattresses Lot/code info: UDI 00887761977853; Serial numbers: W236BP4315, W236BP4320, W236BP4326, W235BP4284, W235BP4294, W236BP4318, W236BP4319, W236BP4323, W236BP4325, W236BP4331, W236BP4333, W236BP4334, W236BP4336, W235BP4270, W235BP4271, W235BP4272, W235BP4278, W235BP4279, W235BP4287, W235BP4291, W235BP4292, W235BP4299, W235BP4307, W235BP4311, W236BP4314, W236BP4321, W236BP4322, W236BP4324, W236BP4329, W236BP4335, W235BP4309, W235BP4313, W215BP3994, W215BP3995, W215BP4002, W215BP4009, W215BP4011, W214BP3979, W214BP3980, W214BP3981, W214BP3982, W214BP3983, W215BP3985, W215BP3986, W215BP3990, W215BP3992, W215BP3993, W215BP3984, W215BP3987, W215BP3988, W215BP3989, W215BP3991, W215BP3996, W215BP4001, W215BP4003, W215BP4005, W215BP4006, W235BP4282, W235BP4285, W235BP4286, W235BP4289, W235BP4293, W235BP4295, W235BP4298, W235BP4300, W235BP4301, W235BP4302, W235BP4303, W235BP4304, W235BP4305, W235BP4306, W235BP4308, W236BP4316, W236BP4317, W236BP4327, W236BP4328, W236BP4330, W236BP4337, W214BP3968, W214BP3969, W214BP3970, W214BP3971, W214BP3972, W214BP3973, W214BP3974, W214BP3975, W214BP3976, W214BP3977, W214BP3978, W215BP3997, W215BP3998, W215BP3999, W215BP4000, W215BP4004, W215BP4007, W215BP4008, W215BP4010, W215BP4012, W235BP4267, W235BP4268, W235BP4269, W235BP4273, W235BP4275, W235BP4276, W235BP4277, W235BP4283, W344BP6702, W344BP6703, W344BP6727, W344BP6728, W344BP6729, W348BP6805, W348BP6806, W348BP6807, W348BP6812, W348BP6813, W348BP6820, W348BP6821, W348BP6827, W348BP6828, W348BP6830, W344BP6688,
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.