Maquet Critical Care AB recall: GETINGE Y SENSOR Module
Maquet Critical Care AB is recalling GETINGE Y SENSOR Module – 9 units. The U.S. Food and Drug Administration published the recall on August 26, 2026; it began on June 30, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | GETINGE Y SENSOR Module |
| Brand | Maquet Critical Care AB |
| Type | Medical devices |
| Classification | Class II |
| Recall date | June 30, 2026 |
| Published by FDA | August 26, 2026 |
| Quantity | 9 units |
| Recall ID | 99439 |
Recalled products
- GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system, for facility use. Maquet Critical Care AB, is a subsidiary of Getinge.
- FDA recall number
- Z-2963-2026
- Codes, lots and dates
- DUI/DI 07325710000304, Serial/Lot Numbers: 21049, 21088, 21089, 21093, 21100, 21103 21108, 21114, 21115.
- Quantity
- 9 units
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99439
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Solna, Sweden
Why it was recalled
The reason the FDA lists: “The module did not undergo electrical safety tests and functional tests during production.”
Where it was sold
Nationwide. Distribution as the FDA records it: “US Nationwide distribution in the states of CA, GA, MN, NY.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99439, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
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About this recall
Is Maquet Critical Care AB GETINGE Y SENSOR Module recalled?
Yes. Maquet Critical Care AB recalled it on June 30, 2026; FDA published it August 26, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
The module did not undergo electrical safety tests and functional tests during production.
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.