Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls Recall Date to: 07/05/2015 |
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Z-0147-2008 - ARCHITECT c16000 Processing Module, for In Vitro Diagnostics; List Number 3L77-01; Affected software: v2.10, v2.11, v2.12, v2.20, v2.20DB, v2.30, v2.60, v3.00 and v3.10; Distributed by Abbott Laborato... | 2 | 11/07/2007 | Abbott Laboratories, Inc |
Z-0146-2008 - ARCHITECT c8000 Processing Module, for In Vitro Diagnostics; List Number 106-01; Affected software: v2.10, v2.11, v2.12, v2.20, v2.20DB, v2.30, v2.60, v3.00 and v3.10; Distributed by Abbott Laboratori... | 2 | 11/07/2007 | Abbott Laboratories, Inc |
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