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Hospira Inc. recalls *** 1) Product labeled in part: List No. 14220-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, CLAVE Y-Site, N
Recalled July 6, 2016 · FDA recall Z-2060-2016 · Hospira
Hazard
Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV administration sets. · FDA Class II
Units
3,920,932 units in total
Sold at
US (Nationwide) Distribution
Description
Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV administration sets.
Product
*** 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 is used as an easy secondary access that allows concurrent and piggyback mode in infusion. It is normally used with a syringe or a secondary IV infusion set.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →