Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm Recalled by Intersurgical Inc Due to When assembling an HME or Filter on this...

Date: April 25, 2018
Company: Intersurgical Inc
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Intersurgical Inc directly.

Affected Products

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

Quantity: 1340

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed to 5 states: IL, NV, NJ, TX, UT

Affected (5 states)Not affected

About Intersurgical Inc

Intersurgical Inc has 11 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report