Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K040796 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Roche ACCU-CHEK Compact Plus Meter Kit, Roche Diagnostics, Indianapolis, IN; REFS 03149137001, 05177... | 2 | 08/11/2009 | Roche Diagnostics Corp. |
ACCU-CHEK Go Care Kit; Catalog number 04470052001. Kit includes an ACCU-CHEK Go meter. | 2 | 08/13/2005 | Roche Diagnostics Corp. |
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