Encore Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street, Gloucester, GL1 2SL, England, U.K.; Models KKB5022-21US and KKB5042-21US. The Encore is designed to be used as a standing and raising aid, it is useful for short transfers from one sitting position to another, and to elev
Check against the official notice below — it lists the full affected range.
Arjo, Inc. is recalling Encore Mobile Patient Lifter models KKB5022-21US and KKB5042-21US due to an exposed metal support bracket that can cause injuries when the knee pad assembly is removed. The company received a limited number of customer reports of injuries related to this hazard. A total of 2,552 units were distributed in the United States, with an additional 4,970 units distributed worldwide across multiple countries including Canada, Australia, Japan, and many European nations.
The recall affects specific serial numbers of the affected models. The source does not specify a remedy for consumers who have this product.
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: 2,552 units in the U.S., 4,970 units in the rest of the world Lot/code info: Models KKB5022-21US, serial numbers 010390894401, 010390894402, 010390894403, 010390894405, 010390894408, 010390894410, 020390958503, 030186208608, 030186208609, 030186208610, 030186208701, 030186208702, 030186208704, 030186208705, 030186208706, 030186208707, 030186208708, 030186208709, 030186208710, 030186208801, 030186208802, 030186208803, 030186208804, 030186208810, 030186208903, 040186294405, 040186453504, 040186453507, 040186453508, 040186453509, 040391134003, 040391134004, 040391134005, 040391134006, 040391134007, 040391134008, 040391134009, 050186453403, 050186453404, 050186453405, 050186453406, 050186453407, 050186453408, 050186453409, 050186453410, 050186453601, 050186453602, 050186453603, 050186453604, 050186453605, 050186453606, 050186453607, 050186453608, 050186453609, 050186453610, 050288869704, 050288869705, 050288869706, 050288869707, 050288869708, 050288869709, 050288869710, 050288888001, 050288888002, 050288888003, 050288888004, 050288888005, 050288888006, 050288888007, 050288888008, 050288888009, 050288888010, 050288913901, 050288913902, 050288913903, 050288913909, 050288913910, 050288914001, 050288914002, 050288914003, 050288914004, 050288914005, 050288914006, 050288914007, 050288914008, 050288914009, 050288914010, 060186453701, 060186453702, 060186453703, 060186453704, 060186453705, 060186453706, 060186453708, 060186453709, 060186453710, 060186453801, 060186453802, 060186453803, 060186453804, 060186453805, 060186453806, 060288914101, 060288914102, 06028891
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.