Medical Device Recalls

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Product Description	Recall Class	FDA Recall Posting Date	Recalling Firm
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Z-2058-2016 - * 1) Product labeled in part: List No. 14212-28; LIFESHIELD; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, Non-Vented, 110 Inch, Non-DEHP; * 2) Product labeled in part: List No. 14254-28; ...	2	06/29/2016	FEI # 3013319212 Hospira Inc.
Z-2059-2016 - *** 1) Product labeled in part: 14951-48; LIFESHIELD; PLUMSET WITH CONVERTIBLE PIERCING PIN, TWO INTEGRAL CLAVE PORTS AND CLAVE ON SECONDARY PORT; NOMINAL LENGTH: 104 IN (264 CM); PRIMING VOLUME: 19 M...	2	06/29/2016	FEI # 3013319212 Hospira Inc.
Z-2062-2016 - *** 1) Product labeled in part: 19683-28; LIFESHIELD; MICRODRIP SOLUSET WITH 1.2 MICRON FILTER 150ML BURETTE PLUMSET, CONVERTIBLE PIN, CLAVE SECONDARY PORT, OPTION-LOK, NON-DEHP; NOMINAL LENGTH: 118 I...	2	06/29/2016	FEI # 3013319212 Hospira Inc.
Z-2061-2016 - *** 1) Product labeled in part: 19734-28; LIFESHIELD; LIFESHIELD LATEX-FREE PLUM SET, MICRODRIP,PP SOLUSET,FILTER, 3 CLAVE PORTS, OPTION-LOK, NON-DEHP; NOMINAL LENGTH: 124 IN (315 IN); PRIMING VOLUME:...	2	06/29/2016	FEI # 3013319212 Hospira Inc.
Z-2060-2016 - *** 1) Product labeled in part: List No. 14220-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, CLAVE Y-Site, Non-Vented, 110 Inch, Non-DEHP; Product Usage: The CLAVE of the secondary port ...	2	06/29/2016	FEI # 3013319212 Hospira Inc.