Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
*** 1) Product labeled in part: List No. 14220-28 Recalled by Hospira Inc. Due to Intravenous fluid may leak at the CLAVE secondary...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Hospira Inc. directly.
Affected Products
*** 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.
Quantity: 3,920,932 units in total
Why Was This Recalled?
Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV administration sets.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hospira Inc.
Hospira Inc. has 245 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report