Covidien recalls Shiley Lo-Pro Oral/Nasal Tracheal Tubes with potential leaks in the cuffed inflation system. Affected units include model REF 86051, 7.0 mm I.D. with specific lot numbers. Contact for replacement or return.
Due to potential leaks associate with the Oral/Nasal Tracheal Tube Cuffed inflation system.
Covidien is recalling Shiley Lo-Pro Oral/Nasal Tracheal Tubes that may leak due to the cuffed inflation system. This could lead to airway complications during medical procedures. Patients and healthcare providers using these tubes should stop using them immediately.
The cuffed inflation system in these tubes may leak, which could cause airway complications during medical procedures. Leaks might lead to inadequate airway protection or other serious issues if the tube is used improperly.
Healthcare providers and patients who use the Shiley Lo-Pro Oral/Nasal Tracheal Tubes for medical procedures are affected. Those with the specific model and lot numbers are at highest risk.
Check for the model number REF 86051 with a 7.0 mm I.D. on the tube. Affected units have lot numbers 22G0343JZX or 22G0344JZX.
Immediately stop using the Shiley Lo-Pro Oral/Nasal Tracheal Tube if it has the model number REF 86051 and lot numbers 22G0343JZX or 22G0344JZX.
The model number is REF 86051 with a 7.0 mm I.D.
Lot numbers 22G0343JZX and 22G0344JZX are affected.
Check for the model number REF 86051 with a 7.0 mm I.D. and lot numbers 22G0343JZX or 22G0344JZX.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1318-2023 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1318-2023 from Covidien. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.