GE Medical Systems recalls Tec 6 Plus and Tec 800 series anesthesia vaporizers with certain reference numbers due to manufacturing issues that may deliver less anesthetic than set. Affected units include specific model numbers and serial numbers.
Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
GE Medical Systems is recalling certain Tec 6 Plus and Tec 800 series anesthesia vaporizers because they may deliver less anesthetic agent than the dial setting indicates. This could lead to inadequate anesthesia during procedures. Affected units have specific reference numbers and serial codes listed in the recall.
The vaporizers have a manufacturing issue that causes them to deliver less anesthetic agent than the dial setting shows. This means the patient might receive less anesthesia than intended, potentially leading to inadequate pain control during surgery or medical procedures.
Healthcare professionals using anesthesia vaporizers for medical procedures are most at risk. Patients receiving anesthesia through these devices could experience inadequate pain management if the vaporizer malfunctions.
Check if your Tec 6 Plus or Tec 800 series anesthesia vaporizer has reference numbers including 1107-9601-000 through 1107-9617-000, 2066835-001, and other specific model numbers listed in the recall. Also check the serial numbers provided in the recall notice.
Verify your vaporizer's reference number and serial number against the list provided in the recall notice.
The vaporizer may deliver less anesthetic agent than the dial setting indicates due to a manufacturing issue.
Check your vaporizer's reference number and serial number against the list of affected models and serial numbers provided in the recall notice.
The recall notice does not specify a remedy, so you should contact GE Medical Systems directly for further instructions.
We’ve drafted a message you can send GE Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0814-2025 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-0814-2025 from GE Medical Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
