GE Medical Systems, LLC 2025-01-15 Health serious FDA
Health · FDA · Recall #FDA-Z-0815-2025
Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO Recall
Issued January 15, 2025 · GE Medical Systems, LLC
In January 2025, GE Medical Systems, LLC recalled the Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
What you should do
- 1 Stop using Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact GE Medical Systems, LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- GE Medical Systems, LLC
- Category
- Health
- Recall date
- January 15, 2025
- Units affected
- Not reported
- Sold at
- US Nationwide. Global Distribution.
- Recall number
- FDA-Z-0815-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- GE Medical Systems, LLC has 12 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.