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Intersurgical Inc recalls Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000
Recalled July 4, 2018 · FDA recall Z-2302-2018 · Intersurgical
Hazard
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. · FDA Class II
Units
1340
Sold at
Distributors in IL, NJ, NV, TX, UT.
Description
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.
Product
Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000
Manufacturer(s)
Intersurgical Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →