Class II — SDI Limited
| Recalling firm | SDI LTD. |
|---|---|
| Registered facility | SDI LTD. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Potential for electrical discharge from unit when unplugged. |
| Product | Dentsply Sirona Capsule Mixer Model No. 5546068 |
| Quantity | 1,444 units |
| 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 |
| Initiated | 2026-07-20 |
| Classified | 2026-08-14 |
| Recall number | Z-2954-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — SDI Limited (Z-2954-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99322/
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