Teleflex recalls Safety Clear Tracheal Tubes with risk of 15mm connector disconnection. Affected models include specific batch numbers. Stop using if you have the recalled product.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling Safety Clear Tracheal Tubes that may disconnect at the 15mm connector. This could lead to breathing issues during medical procedures if the tube becomes disconnected. Affected products have specific batch numbers listed in the recall.
The 15mm connector on the affected tubes can disconnect during use, potentially causing breathing difficulties. This disconnection risk occurs when the tube is being used in medical procedures where continuous air flow is critical.
Healthcare professionals and patients using the recalled tracheal tubes during medical procedures. Those with the specific batch numbers listed in the recall are most at risk.
Check for the product name 'Safety Clear Tracheal Tube, oral/nasal, Magill' with the batch numbers listed in the recall. The unique identifier (UDI/DI) 14026704341495 is also associated with these products.
Look for the batch numbers listed in the recall: 18FG31, 18GT32, and other specific codes.
If you have the recalled product, stop using it immediately to prevent potential disconnection during medical procedures.
The 15mm connector can disconnect from the endotracheal tube, potentially causing breathing issues during medical procedures.
Check for the batch numbers listed in the recall: 18FG31, 18GT32, 18IG03, and other specific codes provided in the record.
Stop using the product immediately and contact Teleflex for further instructions.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1895-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1895-2023 from Teleflex. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
