Medical Device Recalls
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Related Medical Device Recalls |
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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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Z-1686-2017 - Legionella IFA Substrate Slide (IF0951) intended for qualitatively detecting and semi-quantitating human serum antibodies to Legionella pneumophila. | 2 | 03/27/2017 | Focus Diagnostics Inc |
Z-1685-2017 - Legionella IFA (IF0950) intended for qualitatively detecting and semi-quantitating human serum antibodies to Legionella pneumophila. | 2 | 03/27/2017 | Focus Diagnostics Inc |
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