Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
(1) Teleflex Flex tube Recalled by TELEFLEX MEDICAL INC Due to Reports received of torn corrugated breathing tubes.
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 INC directly.
Affected Products
(1) Teleflex Flex tube, Product #20011, sterile; (2) Teleflex Smooth-Flo Flex with Double Swivel, Product #22511, sterile; (3) Teleflex Smooth-Flo Flex with Double Swivel, Product #22512, non-sterile; (4) Teleflex Smooth-Flo Flex, Product #22552, non-sterile.
Quantity: 290,809 eaches
Why Was This Recalled?
Reports received of torn corrugated breathing tubes.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About TELEFLEX MEDICAL INC
TELEFLEX MEDICAL INC has 32 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report