Medical Device Recalls
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31 to 34 of 34 Results
510(K) Number: K980367 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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AEROSET Analyzer | 2 | 05/20/2003 | Abbott Laboratories, Inc |
AEROSET System External Waste Pump | 3 | 05/09/2003 | Abbott Laboratories, Inc |
AEROSET ICT Module, Reagent module for sodium, potassium, and chloride. List number 9D05-01. | 2 | 05/01/2003 | Abbott Laboratories, Inc |
AEROSET Software versions 1.00ER005, catalog number 2-89996-01 and 1.00ER005.2, catalog number 2-899... | 2 | 04/16/2003 | Abbott Laboratories, Inc |
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