Medical Device Recalls
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1 result found
510(K) Number: K052722 |
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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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LifeShield Latex-free Primary I.V. Set, convertible P.P. yellow key slide clamp, backcheck valve, 4 ... | 2 | 02/22/2010 | Hospira Inc. |
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