Tec 820 SEV Anesthesia Vaporizer, Reference Number 1177-9820-SEV
FDA Recall Z-0816-2025 · Posted 2025-01-07
Advertisement
Recalling FirmGE Medical Systems, LLC
Recall StatusOpen, Classified
Product CodeCAD
Date Initiated2024-11-18
Product Quantity928 units
Reason for Recall
Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
Firm Action
An URGENT MEDICAL DEVICE CORRECTION notification letter dated 11/18/24 was sent to customers.
Actions to be taken by Customer/User
You can continue to use the vaporizer in accordance with the instructions in the User Reference Manual (URM) and the actions described below:
1. Perform the Output Concentration Check described in Appendix 1 for every impacted vaporizer (see Affected Product Details in this letter).
" If a vaporizer passes the Output Concentration Check, you can continue to use that vaporizer. GE HealthCare recommends use of anesthetic agent monitoring during vaporizer use.
" If a vaporizer fails the Output Concentration Check, you can continue to use that vaporizer with anesthetic agent monitoring until GE HealthCare corrects the vaporizer.
" If a vaporizer fails the Output Concentration Check and anesthetic agent monitoring is not available, remove the vaporizer from service.
2. Please complete and return the attached Medical Device Notification Acknowledgement Response Form to [email protected]
3. Please ensure all potential staff in your facility are made aware of this safety notification and the recommended actions.
4. Please retain this document for your records.
If you have any questions or concerns regarding this notification, please contact GE HealthCare Service at 1-800-437-1171 or your local Service Representative.
Root Cause
Process control
Distribution Pattern
US Nationwide. Global Distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement