Chorus Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street, Gloucester, GL1 2SL, England, U.K.; Models KKB5060-21US, KKB5062-21US and KKB5080-21US. The Chorus is designed to be used as a standing and raising aid, it is useful for short transfers from one sitting position to anothe
Check against the official notice below — it lists the full affected range.
Arjo, Inc. is recalling Chorus Mobile Patient Lifter models KKB5060-21US, KKB5062-21US, and KKB5080-21US due to an exposed metal support bracket that can cause injuries when the knee pad assembly is removed. The company has received a limited number of customer reports of such injuries. Approximately 1,989 units have been distributed in the United States, with an additional 1,626 units distributed worldwide across numerous countries including Canada, Australia, Japan, and various European nations.
The recall affects specific serial numbers of the KKB5060-21US model and potentially other models in the series. The source document does not specify a remedy for consumers affected by this recall.
Written by software from the official notice below. Not reviewed by a lawyer.
ArjoHuntleigh has received a limited number of customer reports concerning injuries related to an exposed metal support bracket when the proactive knee pad assembly is removed.
Reason for recall: ArjoHuntleigh has received a limited number of customer reports concerning injuries related to an exposed metal support bracket when the proactive knee pad assembly is removed. Distribution: Worldwide Distribution-USA (nationwide) and the countries of Australia, Austria, Belgium, Bermuda, Canada, Cyprus, Czech Republic, Denmark, Dubai, Estonia, Finland, France, Germany, Gibraltar, Great Britain, Greece, Hong Kong, Iceland, Ireland, Israel, Italy, Japan, Kenya, Korea, Luxembourg, the Netherlands, New Zealand, Northern Ireland, Norway, Poland, Portugal, Quatar, Saudi Arabia, Singapore, Quantity: 1,989 units in the U.S., 1,626 units in the rest of the world Lot/code info: Model KKB5060-21US, serial numbers 050186430602, 050186430608, 050186430610, 060186430704, 080186430908, 080186430909, 090186431001, 090186431002, 090186431004, 090186431006, 090186431008, 090186431009, 090186431010, 100186431102, 100186431103, 100186431104, 100186431105, 100186431106, 100186431107, 100186431108, 100186431110, 100186431207, 100186431209, 120186815003, 120186815004, 120186815006, 120186815007, 140186815107, 140186815108, 140186815109, 140186815110, 140186820201, 140186820202, 140186820204, 140186820205, 140186820207, 140186820208, 140186820209, 140186820210, 140186820301, 140186820302, 140186820303, 140186820304, 140186820305, 140186820306, 140186820308, 140186820309, 190084658701, 190084658702, 190084658703, 190084658704, 190084658705, 190084658706, 190084658708, 190084658709, 190084658710, 200084658808, 200084658809, 200084658810, 210084711101, 210084711102, 210084711103, 210084711104, 210084711105, 210084711106, 210084711107, 230084817403, 230084817404, 230084817405, 230084817406, 230084817407, 230084817408, 230084817409, 230084817410, 230084817501, 230084817502, 230084817503, 230084817504, 230084817505, 230084817506, 230084817507, 230084817508, 230084817509, 240084817601, 240084817602, 240084817603, 240084817605, 240084817606, 240084817607, 240084817608, 240084817609, 240084817610, 240084883501, 240084883502, 240084883503, 240084883504, 240084883505, 240084883506, 240084883507, 240084883508, 240084883509, 240084883510, 250084883601, 250084883602, 250084883
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.