Teleflex recalls Flexi-Set Cuffed Endotracheal Tubes with reported disconnections at 15mm connectors. Affected units have specific batch numbers and reference codes. Consumers should check their product details to determine if recalled.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling Flexi-Set Cuffed Endotracheal Tubes and Stylet Sets that have reported disconnections at the 15mm connector. This could lead to breathing issues if the tube becomes disconnected during medical procedures.
The 15mm connector on the endotracheal tube can disconnect during medical procedures. This disconnection could cause breathing problems for patients if the tube is no longer properly connected to the ventilator system.
Healthcare professionals using the affected endotracheal tubes for patient intubation are most at risk. Patients receiving intubation care with the recalled products may experience breathing difficulties if the tube disconnects.
Check for the reference code 504560 on the product packaging. Affected units have specific batch numbers listed in the recall notice, including 18FG03 through 20GT06 and other codes.
Look for the reference code 504560 and the listed batch numbers on the product packaging to determine if your item is affected.
The recall reports disconnections that could cause breathing issues during medical procedures, but the hazard is not described as causing serious injury in normal use.
Check for the reference code 504560 and the specific batch numbers listed in the recall notice, including 18FG03 through 20GT06 and other codes.
The recall does not specify a stop-use action; affected units should be checked for the reference code and batch numbers to determine if they are recalled.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1847-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1847-2023 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.
