Device recall: Tec 6 Plus Anesthesia Vaporizer, Reference Numbers 1107-9601-000, 1107-9602-000, 1107-9603-000, 1107-9604-000…
Class II FDA enforcement event 95855. Recall start date: . Status in the FDA record: Ongoing.
Reason for recall, in the words of FDA
Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
GE Medical Systems, LLC started this device recall on 18 Nov 2024. The firm address in the FDA record is in Waukesha, WI. FDA put the recall in Class II. FDA event 95855 has 5 product records. The first FDA enforcement report date is 15 Jan 2025. The record gives the status Ongoing.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
US Nationwide. Global Distribution.
Recalling firm
GE Medical Systems, LLC, Waukesha, WI.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
5 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-0814-2025 | Tec 6 Plus Anesthesia Vaporizer, Reference Numbers 1107-9601-000, 1107-9602-000, 1107-9603-000, 1107-9604-000, 1107-9610-000, 1107-9612-000, 1107-9616-000, 1107-9617-000, 2066835-001, 2069767-001, 2078800-001, 2091008-001, 2091009-001, M1098876, M1145610, M1220023, M1220854, M1221495, and M1233992 | 1573 units | Class II | Ongoing | 15 Jan 2025 |
| Z-0815-2025 | Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO | 644 units | Class II | Ongoing | 15 Jan 2025 |
| Z-0816-2025 | Tec 820 SEV Anesthesia Vaporizer, Reference Number 1177-9820-SEV | 928 units | Class II | Ongoing | 15 Jan 2025 |
| Z-0817-2025 | Tec 850 ISO Anesthesia Vaporizer, Reference Number 1177-9850-ISO | 1594 units | Class II | Ongoing | 15 Jan 2025 |
| Z-0818-2025 | Tec 850 SEV Anesthesia Vaporizer, Reference Number 1177-9850-SEV | 8319 units | Class II | Ongoing | 15 Jan 2025 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2024
- 970
- Share of these events in Class II
- 87%
- Product records in this event
- 5Median of the firm: 3
- Events of the firm on the register
- 42
Other events of the firm
Official channels
- FDA enforcement report Z-0814-2025The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 95855. https://recallregister.com/fda/ii/95855/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
US Nationwide. Global Distribution.
- What quantity of product is in FDA event 95855?
- The event has 5 product records. The first record gives this quantity:
1573 units
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2024 have the same class?
- 87% of the 970 device events that started in 2024 are in Class II.