SenTec AG recalls
Every recall we track for SenTec AG — 9 in all, from 2019–2023 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from SenTec AG peaked in 2019 (5); 9 since 2017.
All FDA recall records for SenTec AG since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 5 | 0 | 5 |
| 2020 | 0 | 1 | 0 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 2 | 0 | 2 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled SenTec AG product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All SenTec AG recalls
5 shown- Lower riskMedical device
SenTec AG recalls Membrane Changer Single-Use, REF MC, each package contains 3 changers; Membrane Changer Reloadable, REF MC-R, each
SenTec recalls Membrane Changers (MC, MC-R, MC-I) due to potential manufacturing defect that could impact measurement accuracy. Affected units include specific model numbers and serials.
SenTecJul 25, 2023 - Lower riskMedical device
SenTec AG recalls V-Sign Sensor 2, REF VS-A/P/N, a component of Sentec Digital Monitoring System (model SDMS).
SenTec recalls V-Sign Sensor 2 (REF VS-A/P/N) due to potential out-of-box failure after recalibration. Affected units have specific serial numbers and UDI-DI codes.
SenTecMay 2, 2023 - Lower riskMedical device
SenTec AG recalls sentec 24 / MARe-SF Multi-Site Attachment Ring Easy, For sensitive / fragile skin. Used in continuous, noninvasive
SenTec recalls its 24/MARe-SF Multi-Site Attachment Ring for sensitive skin due to weak skin adhesion risk. Affected units have batch #220139.
SenTecAug 22, 2022 - Use cautionMedical device
SenTec AG recalls SenTec Digital Monitor, Model SDM, is a portable stand-alone patient monitor indicated for continuous, noninvasive
SenTec recalls SDM patient monitors sold without isolation transformers for home use. These devices may not meet safety standards, risking electrical hazards. Affected units have specific serial numbers listed.
SenT:ecDec 10, 2020 - Lower riskMedical device
SenTec AG recalls SenTec Standard Starter Set with and without Service Gas (2 changers each) - Product Usage: Is indicated for
SenTec recalls standard starter sets for potential low electrolyte during membrane changes. This may affect CO2 and oxygen monitoring in medical devices. Affected lots listed in the recall notice.
SenTecMay 2, 2019
SenTec AG recall questions
How many recalls has SenTec AG had?
9 recalls from SenTec AG are on record with U.S. safety agencies, from 2019–2023.
What is the most recent SenTec AG recall?
SenTec AG recalls Membrane Changer Single-Use, REF MC, each package contains 3 changers; Membrane Changer Reloadable, REF MC-R, each, dated Jul 25, 2023. Every SenTec AG recall is listed on this page, newest first.
What should I do if I have a recalled SenTec AG product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new SenTec AG recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.