Merit Medical Systems, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2742-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body.

Product Classification:

Class II

Date Initiated: February 2, 2018

Date Posted: August 22, 2018

Recall Number: Z-2742-2018

Event ID: 80650

Reason for Recall:

Supplier manufacturing defect with the syringe plunger tip.

Status: Terminated

Product Quantity: 22,234

Code Information:

Catalog Number: Lot Number: K01-05526P H1258821, K01-07427 H1263015, K01-07477P H1250809 and H1242962, K01-07930P H1246733, MSS011-DG H1246809, K02-00565C H1258361, MSS011-LG H1246810, K02-01260B H1258575 and H1265248, MSS011-PR H1242752, MSS011-R H1242754 and H1255507, K02-01331A H1252652, K04-00748 H1258488 and H1264381, MSS011-Y H1246811, MSS011-YP H1242927, K12-03636 H1258530, and MSS011 H1242750, H1246807 and H1255504.

Distribution Pattern:

Worldwide Distribution: US (nationwide) to states of: AL, AR, AZ, CA, CO, FL, GA, IL, IN, KS, LA, MD, ME, MI, MN, MO, NC, ND, NJ, NM, NY, OH, OR, PA, RI, SC, SD, TB, TN, TX, UT, VA, WI, and WV; and countries of; Canada, Colombia, France, and Italy.

Voluntary or Mandated:

Voluntary: Firm initiated