Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K042330 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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MULTIGENT Acetaminophen for use with Architect/Aeroset Cat. No. 2K99-20. Assay is intended for t... | 2 | 06/27/2012 | Sekisui Diagnostics Llc |
MULTIGENT Acetaminophen, List Number 2K99-20 | 2 | 09/18/2007 | Abbott Laboratories Inc. |
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