FDA Device recall Z-2302-2018
Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000
- FDA Device
- Class II
- terminated
- Published 2018-07-04
On 2018-07-04 the FDA classified a Class II recall of Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000 by Intersurgical, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2302-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-04-25 |
| Published | 2018-07-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Intersurgical |
| Distribution | IL, NJ, NV, TX, UT |
Product
Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000
Reason
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.
Identifiers
| code_info | 0261604, 0671602, 0671603, 0741609, 0751601 , 0821605, 0821606, 0891605, 0891606, 0951609, 0961601, 1751601 , 0011802, 0011803, 0021803, 0081808 and 0161805. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2302-2018%22
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