Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K101677 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Hospira Blood Set, with 200 Micron Filter, 80 Inch, Non-DEHP; an Rx sterile medical device used to a... | 2 | 01/19/2012 | Hospira Inc. |
*** 1) Product labeled in part: List No. 14220-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE P... | 2 | 06/29/2016 | Hospira Inc. |
*** 1) List number 126970465 labeled in part: 12697-65 LifeShield LATEX-FREE HEMA; Y-TYPE BLOOD SET,... | 2 | 03/06/2014 | Hospira Inc. |
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