Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Lubricated Intubating Stylet 6FR that is inserted into an endotracheal Recalled by Cardinal Health Due to A small piece of the stylet sheath has...
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 Cardinal Health directly.
Affected Products
Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is used in surgical or medical emergency facilities. Primarily used on infants and pediatric patients.
Quantity: 104,432 stylets
Why Was This Recalled?
A small piece of the stylet sheath has the potential to shear off upon removal of the stylet from the tracheal tube.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Cardinal Health
Cardinal Health has 75 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report