WalkMed Infusion, LLC: Medical Device Recall in 2015 - (Recall #: Z-0242-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietary name: AFF (Mark I) Volumetric Infusion Pump). Used to pump fluids into a patient in a controlled manner.

Product Classification:

Class II

Date Initiated: October 1, 2015

Date Posted: November 18, 2015

Recall Number: Z-0242-2016

Event ID: 72331

Reason for Recall:

The device might fail to detect air in line while infusing the medication Venofer. This may occur when a drop of Venofer gets stuck in the tubing adjacent to the bubble detector and the Total Volume Limit is programmed higher than the actual bag volume.

Status: Terminated

Product Quantity: 4695 units

Code Information:

Model numbers 300000, 400000

Distribution Pattern:

Distributed in the states of AL, CA, CO, DE, FL, GA, IL, MA, MD, MI, MN, MS, NC, NJ, NM, NV, NY, OH, PA, TN, TX, and WA.

Voluntary or Mandated:

Voluntary: Firm initiated