Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K063866 |
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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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BIO-RAD BioPlex 2200 Syphilis IgG Control Set. Lot # 46636 The BioPlex 2200 Syphilis IgG Control ... | 2 | 06/26/2015 | Bio-Rad Laboratories |
BIOPLEX 2200 SYPHILIS IgG Kit: 100 tests - Catalog No. 665-1450 - manufactured by Bio-Rad Laboratori... | 2 | 06/11/2008 | Bio-Rad Laboratories |
BioPlex 2200 System, Cat. No. 665-1460A containing APF CD SW2_v1., Syphilis IgG IFU Packet contains ... | 3 | 11/09/2007 | Bio-Rad Labroatories Inc. |
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