Medical Device Recalls
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1 result found
510(K) Number: K925058 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Baxter Solution Set for Epidural Use, 110" (2.8 m), Male Luer Lock Adapter; a sterile, single use, n... | 2 | 06/29/2011 |
FEI # 1416980 Baxter Healthcare Corp. |
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