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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| Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel, installed by Pacific Medical Group (... | 1 | 04/19/2021 |
FEI # 3007409280 Pacific Medical Group Inc. |
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