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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 14 Results
510(K) Number: K983212
 
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ARCHITECT i1000SR REF 01L86-01/1L86 and 1L87; ARCHITECT i2000SR REF 03M74-02/3M74; ARCHITECT i2000 R... 2 11/19/2021 Abbott Laboratories
ARCHITECT c4000 REF 02P24-01/2P24, 1P86, 1R24, and 1R25; ARCHITECT c8000 REF 01G06-11/1G06; ARCHITEC... 2 11/19/2021 Abbott Laboratories
ARCHITECT System Software v5.00 and v5.10, List Number 5F48-22 and 5F48-23; Part Number 7-204717-01 ... 2 04/09/2010 Abbott Laboratories, Inc
ARCHITECT i2000 System and ARCHITECT i2000 SR wash buffer and wash zone mechanism grounding kit. ... 2 11/09/2009 Abbott Laboratories, Inc
ARCHITECT i2000sr Processing Module, for in vitro diagnostics; List Number 3M74-01; v2.10, v2.11, v2... 2 06/19/2007 Abbott Laboratories, Inc
ARCHITECT i2000 Processing Module, for in vitro diagnostics; List Number 8C89-01; v2.10, v2.11, v2.1... 2 06/19/2007 Abbott Laboratories, Inc
ARCHITECT i2000 Processing Module, for in vitro diagnostics, List Number 08C89-01; manufactured by A... 2 05/09/2007 Abbott Laboratories, Inc
ARCHITECT i2000SR Processing Module, for in vitro diagnostics, List Number 3M74-01; manufactured by ... 2 05/09/2007 Abbott Laboratories, Inc
ARCHITECT i2000 Processing Module, for in vitro diagnostics, List Number 08C89-01; Temperature Contr... 2 02/07/2007 Abbott Laboratories, Inc
ARCHITECT i2000SR Processing Module, for in vitro diagnostics, List Number 3M74-01; Temperature Cont... 2 02/07/2007 Abbott Laboratories, Inc
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