Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Rusch Greenlite MAC 1 Recalled by Teleflex Medical Due to The pouch may contain the incorrect Rusch Green...
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 Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.
Quantity: 2140 units
Why Was This Recalled?
The pouch may contain the incorrect Rusch Green Lite product size. Pouches that are labeled as containing RUSCH GREEN LITE MAC 1 may instead contain RUSCH GREEN LITE MAC 2.
Where Was This Sold?
US only
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