INARI MEDICAL: Medical Device Recall in 2020 - (Recall #: Z-2299-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/ Aspiration System, UDI: 00850291007079

Product Classification:

Class II

Date Initiated: March 23, 2020

Date Posted: June 17, 2020

Recall Number: Z-2299-2020

Event ID: 85424

Reason for Recall:

The hemostasis valve of aspiration guide catheter devices may fail to seal resulting in a loss of vacuum during thrombus aspiration, which may result the procedure being prolonged as another device must be used or suboptimal thrombus removal if the problem is not detected.

Status: Terminated

Product Quantity: 318

Code Information:

Lot: 20010004, 20010005, 20010008

Distribution Pattern:

U.S Distribution in the states of .: IA, GA, MO, MI, AZ, FL, NJ, MN, LA, PA, AL, OH, NY, WI, CA, TX, TN, NH, IL, NC, CT, CO, OK, OR, IN, MA, VA, KY, WA, MS, SC, UT, SD, ND, AR, ID, DE, including DC.

Voluntary or Mandated:

Voluntary: Firm initiated