Intersurgical Inc recalls Flexible Smoothbore Breathing Circuit with Exhalation Port 2
See all recalls from Intersurgical Inc →Recalled Product
Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000
Hazard / Issue
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.
Issued by
FDA
Affected States: IL, NJ, NV, TX, UT
Lot/Code Info: 0261604, 0671602, 0671603, 0741609, 0751601 , 0821605, 0821606, 0891605, 0891606, 0951609, 0961601, 1751601 , 0011802, 0011803, 0021803, 0081808 and 0161805.
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
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