Every recall we track for SenTec AG — 9 in all — plus the complaints and injury reports the public filed about them.
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.
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.
SenTec recalls its 24/MARe-SF Multi-Site Attachment Ring for sensitive skin due to weak skin adhesion risk. Affected units have batch #220139.
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.
SenTec recalls membrane changer inserts for potential electrolyte imbalance during carbon dioxide monitoring. Affected lots include 180759 to 190277. No remedy specified in recall notice.
SenTec recalls membrane changer sets with lots 180961, 181097, and 190053 due to a 5% chance of reduced electrolyte application during membrane changes. This may affect continuous monitoring of oxygen and carbon dioxide levels in patients.
SenTec recalls neonatal starter sets with potential risk of low electrolyte application during membrane changes. Affected lots include 181089, 190051, 190242, and 181068. No remedy specified in official notice.
SenTec recalls 9-piece Membrane Changer sets for potential low electrolyte application during sensor changes, affecting continuous CO2 and oxygen monitoring in medical patients. No remedy specified in official notice.
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.
