Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC Due to Potential for pilot balloon non-inflation or cuff non-deflation.

Date: December 8, 2022
Company: TELEFLEX LLC
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact TELEFLEX LLC directly.

Affected Products

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation

Quantity: 2,270 units

Why Was This Recalled?

Potential for pilot balloon non-inflation or cuff non-deflation.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About TELEFLEX LLC

TELEFLEX LLC has 139 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report