Intersect ENT, Inc.: Medical Device Recall in 2022 - (Recall #: Z-0458-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044

Product Classification:

Class II

Date Initiated: October 21, 2022

Date Posted: December 14, 2022

Recall Number: Z-0458-2023

Event ID: 91063

Reason for Recall:

Sinus Implant product label displays incorrect product information including: "Straight Delivery System", with incorrect reference number and UDI-DI.

Status: Ongoing

Product Quantity: 611 units

Code Information:

REF: 60044, UDI-DI: M927600440, Lot: 22041901

Distribution Pattern:

US Nationwide distribution including in the states of NC, IL, KS, OR, WI, TX, FL, MN, WY, UT, NY, CA, NJ, OK, MD, HI, MT, TN, MO, IA, MA, AZ, GA, LA, ID, SC, WA, SD, ND, CO, NV.

Voluntary or Mandated:

Voluntary: Firm initiated