Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K142702 |
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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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| Medivance(R) ARCTIC SUN(R) ARCTICGEL(TM) Pads: Description, Catalog Number a) Intrepid ArcticGel S... | 2 | 04/27/2019 |
FEI # 1018233 Bard Medical Division |
| Medivance Neonatal ArcticGel Pads, REF: 31802, 3180202, 31802C | 2 | 03/26/2024 |
FEI # 3003329224 Medivance Inc. |
| Medivance ArcticGel Small Pad Kit - a box containing a single foil pouch, which contains a set of fo... | 2 | 12/20/2017 |
FEI # 1018233 C.R. Bard, Inc. |
| Medivance ArcticGel Neonatal Pad The pad is designed to fit into an incubator and provide whole b... | 3 | 08/05/2016 |
FEI # 1018233 C.R. Bard, Inc. |
| BARD ArcticGel Pads Product Usage: The Arctic Sun Temperature Management System is intended for ... | 2 | 04/14/2016 |
FEI # 1018233 C.R. Bard, Inc. |
| Arctic Sun ArcticGel Pads - Medium, Product Code 317-07 | 3 | 02/12/2018 |
FEI # 1018233 C.R. Bard, Inc. |
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