# FDA recall Z-2302-2018

> **Intersurgical Inc** · Class II · device recall initiated 2018-04-25.

## Product

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

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-2302-2018
- **Recalling firm:** Intersurgical Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-04-25
- **Report date:** 2018-07-04
- **Termination date:** 2019-04-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** E. Syracuse, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2302-2018

## Citation

> AI Analytics. FDA recall Z-2302-2018. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-2302-2018. Source: US FDA. Licensed CC0.

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