Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Tec 820 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to Due to a manufacturing issue, certain Tec 6...
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 GE Medical Systems, LLC directly.
Affected Products
Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO
Quantity: 644 units
Why Was This Recalled?
Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE Medical Systems, LLC
GE Medical Systems, LLC has 146 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report