WalkMed Infusion, LLC: Medical Device Recall in 2016 - (Recall #: Z-2221-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Spike Set, 12" Microbore SPM-12. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.

Product Classification:

Class II

Date Initiated: June 14, 2016

Date Posted: July 27, 2016

Recall Number: Z-2221-2016

Event ID: 74437

Reason for Recall:

WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton Administration Sets Due to the Potential Presence of Particulate In or On the Administration Sets.

Status: Terminated

Product Quantity: 37 cases

Code Information:

Product Number: 020-204840. Lot Number: 1504031D

Distribution Pattern:

US Nationwide Distribution in the states of AL, AZ, CA, FL, IL, MA, MS, NJ, NV, NY, OH, PA, TN, UT, and WA.

Voluntary or Mandated:

Voluntary: Firm initiated