Medical Device Recalls
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1 result found
Recall Date to: 12/01/2015 510(K) Number: K032417 |
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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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Sierra Pre-Filled, Heparin Lock Flush Solution USP, 100 units/ml in 0.9% Sodium Chloride 120/Case, C... | 1 | 01/30/2008 | AM2 PAT INC |
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