Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K103224 |
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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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*** 1) Product labeled in part: List No. 14212-28; LIFESHIELD; PLUM Y-TYPE BLOOD SET; 200 Micron Fil... | 2 | 06/29/2016 | Hospira Inc. |
List No. 14212-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, Non-Vented, 110 Inch, Non-D... | 1 | 08/05/2013 | Hospira Inc. |
Hospira Primary Microbore Gemstar Split Set, Integral PAV, Yellow Striped Tubing, 110 Inch, Non-DEHP... | 2 | 04/19/2011 | Hospira Inc. |
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