Medical Device Recalls
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31 to 31 of 31 Results
510(K) Number: K133532 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Alaris SpO2 Module Model 8210 and Model 8220 - Product Usage: is intended to provide trained healthc... | 2 | 08/19/2020 |
FEI # 2016493 CareFusion 303, Inc. |
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