Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected models include REF 112082100 with certain batch numbers. 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 endotracheal tubes with a specific model and batch numbers because reports indicate the 15mm connector may disconnect. This could lead to breathing difficulties during medical procedures if the tube becomes disconnected.
The 15mm connector on the affected endotracheal tubes may become disconnected during use. This disconnection could cause breathing difficulties for patients during medical procedures, especially in critical situations.
Healthcare professionals and medical facilities using the recalled endotracheal tubes are most at risk. Patients receiving these tubes during procedures could face breathing issues if the connector disconnects.
Check for the model number REF 112082100 on the tube. Affected units have specific batch numbers listed in the recall notice, including 18GG13 through KME23A3169.
Look for the model number REF 112082100 and the listed batch numbers on the tube.
Teleflex reports of disconnection of the 15mm connector from the endotracheal tube for the affected products.
Affected batch numbers include 18GG13, 18JG24, 18JG36, 18JT06, 18KG10, 18LG06, 19AG36, 19CG02, 19GT16, 19GT59, 19IT33, 19JT56, 19KT14, 19KT49, 20AT01, 20AT22, 20BG18, 20DT18, 20DT19, 20ET17, KME20H2141, KME20K1809, KME20K2553, KME20L0335, KME20M1341, KME20M2113, KME21A2342, KME21A2668, KME21C0017, KME21F2252, KME21F2345, KME22B1777, KME22B1881, KME22C0019, KME22C0063, KME22C0327, KME22E2679, KME22F0401, KME22H0209, KME22H2251, KME22J2931, KME22J3329, KME22L0218, KME22L0219, KME22L2730, KME22L2731, KME23A2196, KME23A2539, KME23A3169.
Check the product details to see if it is affected. If it is, contact Teleflex 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-1894-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1894-2023 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.
