Medical Device Recalls
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1 result found
510(K) Number: K052828 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ICU Medical, Transpac IV Monitoring Kit With Safeset Reservoir and Blood Sampling Port, 60" Tubing, ... | 2 | 03/28/2019 | ICU Medical, Inc. |
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