FDA Class II · Medical device · August 26, 2026
Dentsply Sirona Capsule Mixer Model No recall — SDI Limited
Potential for electrical discharge from unit when unplugged.
Official ID Z-2954-2026 · Official record ↗
SDI recalls
Recall found. SDI is named in FDA Class II recall Z-2954-2026 covering Dentsply Sirona Capsule Mixer Model No. Hazard: Potential for electrical discharge from unit when unplugged. Identifying details: UDI:9336472005542; Serial Numbers 0003-1533. Status: Ongoing.
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All SDI recalls
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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.