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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
Related Medical Device Recalls Recall Date to: 08/28/2014
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Product Description
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FDA Recall
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Z-1947-2012 - 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 stand... 2 07/06/2012 Arjo, Inc. dba ArjoHuntleigh
Z-1949-2012 - Sara Plus Mobile Patient Lifter; manufactured for Arjo by Medibo Medical Products N.V., Heikant 5, B-3930 Hamont-Achel, Belgium; Models HEP0001-US and HEP1001-US. The Sara Plus is a standing and ra... 2 07/06/2012 Arjo, Inc. dba ArjoHuntleigh
Z-1948-2012 - 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 u... 2 07/06/2012 Arjo, Inc. dba ArjoHuntleigh
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