Fresh Recalls

Dentsply Sirona Capsule Mixer Model No: recall status

Notice names this product. SDI’s Dentsply Sirona Capsule Mixer Model No is named in FDA Class II recall Z-2954-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Potential for electrical discharge from unit when unplugged. Identifying details: UDI:9336472005542; Serial Numbers 0003-1533. Units affected: 1,444 units. Status: Ongoing.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Dentsply Sirona Capsule Mixer Model No
Company / brand
SDI
Lot / serial / date codes
UDI:9336472005542; Serial Numbers 0003-1533
Distribution
US: AK AL AR AZ CA CO CT DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC NE NH NJ NM NV NY OH OK OR PA RI SC SD TN TX UT VA VT WA WI WV OUS: None
Agency product description and boundaries

Dentsply Sirona Capsule Mixer Model No. 5546068

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

Brand
SDI

Recalls naming this model

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.

Company / brand: SDI recalls

Affected product: Dentsply Sirona Capsule Mixer Model No recall status

Official ID Z-2954-2026 · Official record ↗

See all SDI recalls →

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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.