GE Healthcare Recalls Anesthetic Cassettes Due to Non-Conforming Devices
GE Healthcare recalls specific anesthetic cassettes (model 1100-9034-000) that may be nonconforming due to improper service center evaluation. Affected units have lot numbers BGBQ00675 or BGBQ01187.
Recall notice
Non-Conforming devices were shipped from the service center without proper evaluation and therefore may be nonconforming.
Contact the company
What happened, in plain English
GE Healthcare is recalling certain anesthetic cassettes that were shipped without proper evaluation, potentially making them nonconforming. This could affect medical devices used in anesthesia delivery. Read more at govinfonow.com/recall/72905-ge-healthcare-recalls-anesthetic-cassettes-due-to-non-conforming-devices.
Source Summary by GovInfoNow · govinfonow.com/recall/72905-ge-healthcare-recalls-anesthetic-cassettes-due-to-non-conforming-devices · Updated September 17, 2026 · FDA enforcement record: FDA #Z-1199-2018
Cite this page
“GE Healthcare Recalls Anesthetic Cassettes Due to Non-Conforming Devices.” GovInfoNow, updated September 17, 2026. https://govinfonow.com/recall/72905-ge-healthcare-recalls-anesthetic-cassettes-due-to-non-conforming-devices. Based on FDA recall #Z-1199-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1199-2018%22&limit=1).
Why it’s dangerous
The cassettes were shipped from the service center without proper evaluation, which may result in nonconforming devices. Nonconforming devices could lead to improper anesthesia delivery if used in medical procedures.
Who’s affected
Healthcare providers using the recalled cassettes for anesthesia delivery are most at risk. Patients receiving anesthesia through these devices could be affected if the cassettes are nonconforming.
How to tell if you have this one
Check for model number 1100-9034-000 with lot numbers BGBQ00675 or BGBQ01187. These cassettes are used for delivering anesthetic agents in medical settings.
- Brand
GE Healthcare- Category
Medical device
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
US Distribution to states of: AZ, IL NC, NH and PA.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1198-2018 | DATEX-OHMEDA TEC 7 ANESTHESIA VAPORIZER Is designed for the metered delivery of specific inhalation anesthetic agents for use in continuous flow techniques of inhalation anesthesia.; Model # M1107626 Mfg. Lot or Serial #: BEJN05568, BEJM03853, BEJM04539, BEJN05793, BEJP01947, BEJP03924, BEJP04380, BEJP08533, BEJU06631, BEJN06095, BEJP04706, BEJU05053, BEJM04542, BEJM04881, BEJM04901, BEJN07748, BEJN07849, BEJP03230, BEJP03239, BEJP03559, BEJP03984, BEJP05309, BEJP05347, BEJP05825, BEJP05834, BEJP05978, BEJP08567, and BEJP09304. | 28 |
| Z-1199-2018 | DATEX-OHMEDA AISYS CS2 ALADIN2 CASSETTE Cassettes are intended to be used to deliver anesthetic agent.; Model 1100-9034-000 Mfg. Lot or Serial # BGBQ00675 and BGBQ01187 | 2 |
What to do — step by step
Check Product Details
Identify the model number (1100-9034-000) and lot numbers (BGBQ00675 or BGBQ01187) to confirm if your cassette is affected.
Where it went and when
Where it was distributed
Distributed in 5 states.
FDA distribution: “US Distribution to states of: AZ, IL NC, NH and PA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, Illinois, New Hampshire, North Carolina, Pennsylvania.
Recall timeline
FDA terminated this recall 2.5 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-1199-2018 (October 4, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1199-2018 to see it in context.
- Plain-language summary written by qwen3:4b on September 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.