Hospira Inc.: Medical Device Recall in 2014 - (Recall #: Z-1479-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

LifeShield LATEX-FREE HemoSet 100 mL Burette I.V. PlumSet, Nonvented, 105 inch with Prepierced Reseals, OPTION-LOK and Inline Dual Channel Cassette. For administration of blood and blood bags for use with Plum Series Infusers.

Product Classification:

Class II

Date Initiated: February 25, 2014

Date Posted: April 30, 2014

Recall Number: Z-1479-2014

Event ID: 67722

Reason for Recall:

Hospira identified an incorrect lower lid (set component) had been supplied and was being used during the manufacturing process of list number 11241-03, a HemoSet containing a burette and blood filter, intended for infusion of blood/blood products. In a gravity delivery, the correct lower lid dispenses 15 drops per mL and the incorrect lower lid found dispenses 10 drops per mL.

Status: Terminated

Product Quantity: 3,893 sets

Code Information:

Product List Number: 112410403; Lot Numbers: 280055H, 341005H

Distribution Pattern:

US Distribution including the states of FL, IA,IN, KS, KY, ME, MO, MT, PA, TN, TX, UT, VA and WA.

Voluntary or Mandated:

Voluntary: Firm initiated