Medical Device Recalls
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91 to 96 of 96 Results
Product: pcr |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Cobas KRAS Mutation Test for In Vitro Diagnostic Use Product Usage: Usage: The Cobas KRAS Mutat... | 3 | 08/08/2012 | Roche Molecular Systems, Inc. |
Factor II (Prothrombin) G20210A Kit Light Cycler Instrument; Manufactured in Germany for Roche Molec... | 2 | 06/14/2011 | Roche Molecular Systems, Inc. |
Factor V Leiden Kit Light Cycler Instrument; Manufactured in Germany for Roche Molecular Systems, In... | 2 | 06/14/2011 | Roche Molecular Systems, Inc. |
Knee Components: ROTULE "913" D=32 , Part Number PGA00030, Lot Number X02383380 INSERT TIBIAL "913... | 2 | 10/31/2012 | Wright Medical Technology Inc |
Zyston® Transform Instrument Case. Model Number PCR8200-2101. Device labeled sterile. | 2 | 08/11/2016 | Zimmer Biomet Spine, Inc |
Zyston® Transform Implant Kit. Model Number PCR8200-3101. Device labeled sterile. | 2 | 08/11/2016 | Zimmer Biomet Spine, Inc |
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