Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K111353 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ACCU-CHEK Aviva Combo Blood Glucose Meter (as a part of the ACCU-CHEK Aviva Combo System)\ The AC... | 2 | 11/22/2013 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
| ACCU-CHEK Spirit Combo insulin infusion pump sold as part of Accu-Chek Combo System Product Usage... | 2 | 10/29/2014 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
| AccuChek Spirit Combo insulin infusion pump sold as part of Accu-Chek Combo System. | 2 | 06/09/2015 |
FEI # 3011393376 Roche Diabetes Care, Inc. |
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