Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K242117 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| LifeShield Drug Library Management (DLM); LifeShield Infusion Safety Software Suite v2.2 List Nu... | 2 | 12/19/2025 | ICU Medical, Inc. |
| LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software Suite v2.2 Product ... | 2 | 12/19/2025 | ICU Medical, Inc. |
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