Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K983212 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ARCHITECT i2000 System and ARCHITECT i2000 SR wash buffer and wash zone mechanism grounding kit. ... | 2 | 11/09/2009 | Abbott Laboratories, Inc |
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 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 |
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