Hospira Inc.: Medical Device Recall in 2017 - (Recall #: Z-1016-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP, Latex-Free Intended use: For the administration of drugs and solutions to a patient's vascular system through a vascular access device.

Product Classification:

Class II

Date Initiated: February 19, 2013

Date Posted: January 18, 2017

Recall Number: Z-1016-2017

Event ID: 64220

Reason for Recall:

Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore Extension Set, 59 inch with Spin Lock Collar, Non-DEHP, identified above due to a confirmed customer report of an occlusion of solvent in the male luer lock. This occlusion has the potential to prevent the set from being primed for use and cause a delay in therapy.

Status: Terminated

Product Quantity: 48,050 units

Code Information:

Product List Number: 14699-28; Lot Number: 17-077-NS

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated