Flexible Smoothbore Breathing Circuit with Exhalation recall
Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000
Why was Flexible Smoothbore Breathing Circuit with Exhalation 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
0261604, 0671602, 0671603, 0741609, 0751601 , 0821605, 0821606, 0891605, 0891606, 0951609, 0961601, 1751601 , 0011802, 0011803, 0021803, 0081808 and 0161805.
- Product
- Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000
- Recalling firm
- Intersurgical Inc
- Quantity
- 1340
- Distribution
- Distributors in IL, NJ, NV, TX, UT.
- Recall date
- July 4, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)