Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K131029 |
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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 Aviva Plus Test Strip, Blood Glucose Monitoring System, Model numbers: 06908152001, 069082... | 2 | 08/26/2021 | Roche Diabetes Care, Inc. |
Accu-Chek Aviva Plus Retail Strips 50 ct - intended for Blood Glucose Monitoring System Catalog Num... | 2 | 02/05/2020 | Roche Diabetes Care, Inc. |
Accu-Chek Aviva Plus Health Network Strips- intended for Blood Glucose Monitoring System Catalog N... | 2 | 02/05/2020 | Roche Diabetes Care, Inc. |
Accu-Chek Performa Test Strip, Blood glucose monitoring system, Catalog no. 07299702001 Product U... | 2 | 05/09/2018 | Roche Diabetes Care, Inc. |
Accu-Chek Aviva Plus Test Strip, Blood glucose monitoring system, Catalog nos. 06908217001, 06908268... | 2 | 05/09/2018 | Roche Diabetes Care, Inc. |
Accu-Chek Inform II Test Strip, Whole blood glucose test system, Catalog no. 05942861001 Product ... | 2 | 05/09/2018 | Roche Diabetes Care, Inc. |
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