[Recalled] Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082075 — Reports of disconnection of the 15mm connector from the endotracheal tube (ET t… | FDA 2023-05-25

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).

Read the full official notice →

Related recalls from TELEFLEX LLC

• Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170085 — Class I
• Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382035 — Class I
• Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382055 — Class I
• Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150055 — Class I
• Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181055 — Class I
• Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090 — Class I

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.