Medical Device Recalls
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1 result found
Recall Number: Z-2235-2025 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 25). Pro... | 2 | 08/01/2025 |
FEI # 3014732157 Fresenius Kabi USA, LLC |
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