Eleganza 5 (AC powered adjustable bed), Item Numbers: a) 1GE512055-40, b) 1GE512055-45, c) 1GE512055-85, and d) 1GE512055-95 - Product Usage: Eleganza 5 is a positionable bed for intensive care. Its purpose is to support patient and to facilitate treatment and manipulation with patient for nursing p
Check against the official notice below — it lists the full affected range.
Linet Spol. S.r.o. is recalling 518 units of the Eleganza 5 AC-powered adjustable bed with item numbers 1GE512055-40, 1GE512055-45, 1GE512055-85, and 1GE512055-95 that were distributed nationwide in the United States. The beds were distributed under specific lot codes associated with each item number. A component in the side rail mechanism may malfunction, causing the side rail to either fail to lock properly when in the upper position or become stuck in the upper position.
The recall notice does not specify a remedy for consumers who own affected units.
Written by software from the official notice below. Not reviewed by a lawyer.
A component used within the side rail mechanism may malfunction, resulting in the side rail either not locking properly in the upper position or the side rail becoming stuck in the upper position.
Reason for recall: A component used within the side rail mechanism may malfunction, resulting in the side rail either not locking properly in the upper position or the side rail becoming stuck in the upper position. Distribution: US Nationwide distribution. Quantity: 518 units Lot/code info: a) 1GE512055-40: 20170042941, 20170042942, 20170042943, 20170042944, 20170042945, 20170042946, 20170043764, 20170043765, 20170043766, 20170043767, 20170043768, 20170043769, 20170043770, 20170043771, 20170043772, 20170043773, 20170043774, 20170043775 b) 1GE512055-45: 20170055478, 20170055479, 20170055480, 20170055481, 20170055482, 20170055483, 20170055484, 20170055485, 20170055486, 20170055487, 20170055488, 20170055489, 20170055490, 20170056038, 20170056039, 20170056040, 20170056041, 20170056042, 20170056043, 20170056044, 20170056045, 20170056046, 20170056047, 20170056048, 20170056049, 20170056050, 20170056051, 20170056052, 20170056053, 20170056054, 20170056055, 20170056056, 20170056527, 20170056528, 20170056529, 20170056530, 20170056531, 20170056532, 20170056533, 20170056534, 20170056535, 20170056536, 20170056537, 20170056538, 20170056539, 20170056540, 20170056541, 20170056542, 20170056543, 20170056544, 20170056545, 20170056546, 20170058170, 20170058171, 20170058172, 20170058173, 20170058174, 20170058175, 20170058176, 20170058177, 20170058178, 20170058179, 20170058180, 20170058181, 20170058182, 20170058183, 20170058184, 20170058185, 20170058186, 20170058187, 20170058188, 20170058189, 20170058190, 20170058191, 20170058192, 20170058193, 20170058194, 20170058195, 20170059025, 20170059026, 20170059027, 20170059028, 20170059029, 20170059030, 20170059031, 20170059032, 20170059033, 20170059034, 20170059035, 20170059036, 20170059037, 20170059038, 20170059039, 20170059040, 20170059041
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.