Medical Device Recalls
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31 to 34 of 34 Results
510(K) Number: K133532 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Alaris EtCO2 Module Model 8300 - Product Usage: is intended to provide trained healthcare caregivers... | 2 | 08/19/2020 | CareFusion 303, Inc. |
Alaris PCA Module Model 8120 - Product Usage: is intended to provide trained healthcare caregivers a... | 2 | 08/19/2020 | CareFusion 303, Inc. |
Alaris Syringe Module Model 8110 - Product Usage: is intended to provide trained healthcare caregive... | 2 | 08/19/2020 | CareFusion 303, Inc. |
Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers ... | 2 | 08/19/2020 | CareFusion 303, Inc. |
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