Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K983212 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ARCHITECT i2000SR Processing Module, for in vitro diagnostics, List Number 3M74-01; Temperature Cont... | 2 | 02/07/2007 |
FEI # 1628664 Abbott Laboratories, Inc |
| ARCHITECT Processing Module, manufactured by Abbott Laboratories, Irving, Texas | 2 | 07/20/2004 |
FEI # 1628664 Abbott Laboratories, Inc |
| The ARCHITECT i2000, Clinical Chemistry Analyzer, Manufactured by Abbott Laboratories, Irving, Texas | 2 | 12/24/2003 |
FEI # 1628664 Abbott Laboratories, Inc |
| ARCHITECT Processing Module, List number 8C89-01, manufactured by Abbott Laboratories, Irving, Texas | 2 | 08/13/2003 |
FEI # 1628664 Abbott Laboratories, Inc |
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