Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured Recalled by Teleflex Medical Due to Product size listed on the labeling is incorrect.
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 Medical directly.
Affected Products
Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel and aluminum rods that are coated with a blue PVC or polypropylene outer covering and are designed to be placed inside an endotracheal tube to obtain a desired shape during intubation.
Quantity: 21,690 eaches
Why Was This Recalled?
Product size listed on the labeling is incorrect.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teleflex Medical
Teleflex Medical has 204 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report