Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K052052 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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*** 1) Product labeled in part: 19734-28; LIFESHIELD; LIFESHIELD LATEX-FREE PLUM SET, MICRODRIP,PP S... | 2 | 06/29/2016 | Hospira Inc. |
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