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FDA (Device enforcement)Recalled 2022-06-24class ii

Baxter Healthcare Corporation: Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.

Is my product affected?

Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.

  • UPC 00887761977945

Check against the official notice below — it lists the full affected range.

What happened

Baxter Healthcare Corporation is recalling 136 Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattresses due to a potential failure in the Microclimate Management feature, which is designed to pull heat and moisture away from patients. The failure could reduce the performance of this feature and increase the risk of pressure ulcer development in patients using the affected mattresses. The recalled mattresses have been distributed worldwide, including in 27 U.S. states, Canada, and to government facilities.

The specific serial numbers affected by this recall are listed in the recall notice. The source document does not specify a remedy or instructions for what affected consumers should do.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

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.

Details from the source

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: 136 mattresses Lot/code info: UDI 00887761977945; Serial numbers: W238BP4338, W238BP4339, W238BP4340, W238BP4341, W238BP4342, W238BP4344, W238BP4345, W238BP4347, W238BP4348, W355BP6966, W355BP6978, W355BP6979, W355BP6980, W355BP6981, W355BP6982, W355BP6986, W355BP6987, W355BP6988, W355BP6989, W355BP6990, W357BP6994, W357BP6996, W357BP6997, W357BP6998, W357BP7006, W357BP7007, W357BP7009, W357BP7012, W357BP7015, W357BP7016, W357BP7017, W357BP7018, W357BP7019, W357BP7021, W357BP7022, W357BP7023, W357BP7024, W357BP7025, W357BP7026, W357BP7027, W354BP6891, W354BP6892, W354BP6897, W354BP6898, W354BP6899, X003BP7030, X003BP7031, X003BP7036, X003BP7037, X003BP7039, X003BP7040, X003BP7041, X003BP7047, X003BP7049, X003BP7050, X005BP7090, X005BP7091, X005BP7096, X005BP7097, X005BP7098, W354BP6921, W354BP6922, W354BP6923, W354BP6931, W354BP6932, X005BP7087, X005BP7088, X005BP7089, X005BP7094, X005BP7095, W354BP6910, W354BP6911, W354BP6918, W354BP6936, W354BP6939, W355BP6945, X003BP7055, X003BP7057, X005BP7059, X005BP7060, X005BP7061, X005BP7064, X005BP7065, X005BP7066, X005BP7067, X005BP7083, X005BP7086, X005BP7093, X005BP7104, X005BP7106, X005BP7110, X005BP7111, W354BP6908, W354BP6909, W354BP6916, W354BP6917, W354BP6919, W354BP6920, W354BP6924, W354BP6925, W354BP6926, W354BP6927, W354BP6928, W354BP6929, W354BP6933, W354BP6934, W354BP6935, W354BP6940, W354BP6941, W354BP6942, W355BP6944, W355BP6946, W355BP6948, W355BP6949, W355BP6950, W355BP6951, W355BP6952, W355BP6953, W355BP6955, W355BP6956, W355BP6957, W355BP6958,

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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