Medical Device Recalls
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1 result found
510(K) Number: K092938 |
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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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HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION, USP) 100 USP units per 10 mL (10 USP units per mL), Single... | 2 | 01/29/2015 | Fresenius Kabi USA, LLC |
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