Teleflex recalls Safety Clear Tracheal Tubes with risk of 15mm connector disconnection. Affected models include specific batch numbers and UDI/DI codes. Consumers should check their product details.
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.
The 15mm connector can become disconnected from the endotracheal tube during use. This disconnection could cause breathing difficulties or require immediate reconnection, which may be difficult in emergency situations.
Healthcare professionals using the tracheal tubes for medical procedures are most at risk. Patients receiving these tubes during surgery or critical care may be affected.
Check for the product name 'Safety Clear Tracheal Tube, oral/nasal, Magill' with the specific batch numbers listed in the recall notice. The UDI/DI code 14026704341518 is also associated with these products.
Identify your product by checking the batch numbers or UDI/DI code listed in the recall notice.
The recall is due to reports of the 15mm connector disconnecting from the endotracheal tube, which could cause breathing issues during medical procedures.
Check for the product name 'Safety Clear Tracheal Tube, oral/nasal, Magill' with batch numbers 18GG15 through 20BT51 or UDI/DI code 14026704341518.
The recall does not specify a remedy, so contact Teleflex directly for guidance on next steps.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1897-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1897-2023 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.
