SDI Limited Capsule Mixer Model 554: Electrical Discharge Risk
Dentsply Sirona Capsule Mixer Model 5546068 may cause electrical discharge when unplugged. Affected units have UDI:9336472005542 or serial numbers 0003-1533. Stop using immediately to avoid electrical hazards.
Stop using this now
Potential for electrical discharge from unit when unplugged.
What happened, in plain English
SDI Limited is recalling Dentsply Sirona Capsule Mixer Model No. 5546068 due to potential electrical discharge when unplugged. This could cause electrical hazards if the device is not properly handled after unplugging. Read more at govinfonow.com/recall/697861-sdi-limited-capsule-mixer-model-554-electrical-discharge-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/697861-sdi-limited-capsule-mixer-model-554-electrical-discharge-risk · Updated September 14, 2026 · FDA enforcement record: FDA #Z-2954-2026
Cite this page
“SDI Limited Capsule Mixer Model 554: Electrical Discharge Risk.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/697861-sdi-limited-capsule-mixer-model-554-electrical-discharge-risk. Based on FDA recall #Z-2954-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2954-2026%22&limit=1).
Why it’s dangerous
The mixer may discharge electricity when unplugged, creating a risk of electrical shock or damage to nearby objects. This hazard occurs because the electrical components can become energized when disconnected from power.
Who’s affected
Users of the Dentsply Sirona Capsule Mixer Model No. 5546068 with UDI:9336472005542 or serial numbers 0003-1533 are affected. Dental professionals using this mixer are most at risk due to potential electrical discharge.
How to tell if you have this one
Check for the model number 5546068 on the device. Affected units have a unique device identifier (UDI) of 9336472005542 or serial numbers starting with 0003-1533.
- Brand
SDI Limited- Category
Medical device
What to do — step by step
Stop Using It Now
Immediately stop using the Dentsply Sirona Capsule Mixer Model No. 5546068 if it has the UDI 9336472005542 or serial numbers 0003-1533.
Where it went and when
Where it was distributed
Distributed in 48 states.
FDA 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” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin.
Recall timeline
FDA published this recall 37 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2954-2026 (July 20, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2954-2026 to see it in context.
- Plain-language summary written by qwen3:4b on September 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.