Intersurgical Inc: Medical Device Recall in 2018 - (Recall #: Z-2302-2018)

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:

Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000

Product Classification:

Class II

Date Initiated: April 25, 2018

Date Posted: July 4, 2018

Recall Number: Z-2302-2018

Event ID: 80250

Reason for Recall:

When assembling an HME or Filter on this breathing circuit the tubing may be pushed up and inadvertently cover or block the exhalation port. This could potentially pose a serious health risk to the patient.

Status: Terminated

Product Quantity: 1340

Code Information:

0261604, 0671602, 0671603, 0741609, 0751601 , 0821605, 0821606, 0891605, 0891606, 0951609, 0961601, 1751601 , 0011802, 0011803, 0021803, 0081808 and 0161805.

Distribution Pattern:

Distributors in IL, NJ, NV, TX, UT.

Voluntary or Mandated:

Voluntary: Firm initiated