Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm received reports indicating that the laser...
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
RUSCH LASERTUBE (Rubber), Order No. : 102004-000060, REF 102004, SIZE I.D. mm 6,0
Quantity: 4312 units
Why Was This Recalled?
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
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