Merit Medical Systems, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1911-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992209 Version A, Sterile EO, Rx Only

Product Classification:

Class II

Date Initiated: April 22, 2023

Date Posted: June 21, 2023

Recall Number: Z-1911-2023

Event ID: 92301

Reason for Recall:

There is a potential that valve assemblies will not open. preventing fluid from draining.

Status: Ongoing

Product Quantity: 670 units

Code Information:

Lot # I2533611, I2546597, I2559292, I2548163 & I2578001; UDI-DI: 00884450394908

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY, Puerto Rico and the countries of France, United Kingdom, Mexico.

Voluntary or Mandated:

Voluntary: Firm initiated