Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0222-2007 - NOW Legionella Urinary Antigen Test. 22 test kit. For In Vitro Diagnostic Use Product Code: 852-000 | 2 | 11/29/2006 | Inverness Medical Professional Diagnostics |
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