HeartSine® Samaritan® PAD SAM 350P/SAM 360P/SAM 500P - Membrane Tail — recall 82380
Health Canada — Medical Devices · Canada · 2026-07-23 · Type II
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Reported risk: Stryker has recently identified an issue with the membrane tail, an internal component, which could cause an intermittent fault. This failure could occur at any point when the device is holding a charge in preparation to deliver therapy, while delivering a shock, or after shock delivery. The device becomes inoperable after the failure occurs.
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