Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K121679 |
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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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Accu-Chek Inform II Test Strip, Whole Blood Glucose Test System, Model number 05942891001 | 2 | 08/26/2021 | Roche Diabetes Care, Inc. |
Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System ... | 2 | 03/14/2016 | Roche Diagnostics Operations, Inc. |
ACCU-CHEK Inform II Blood Glucose Monitoring System bar code scanner. Used with the ACCU-CHEK In... | 2 | 04/15/2013 | Roche Diagnostics Operations, Inc. |
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