Integra LifeSciences Corp. (NeuroSciences): Medical Device Recall in 2025 - (Recall #: Z-1724-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.

Product Classification:

Class II

Date Initiated: April 4, 2025

Date Posted: May 14, 2025

Recall Number: Z-1724-2025

Event ID: 96672

Reason for Recall:

Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.

Status: Ongoing

Product Quantity: 6 units

Code Information:

Model No. BC1040AZ; UDI: 20705031063157; Lot No. 240716A-PC.

Distribution Pattern:

US Nationwide distribution in the states of TX, MT, AL & OK.

Voluntary or Mandated:

Voluntary: Firm initiated