# FDA recall Z-2954-2026

> **SDI Limited** · Class II · device recall initiated 2026-07-20.

## Product

Dentsply Sirona Capsule Mixer  Model No. 5546068

## Reason for recall

Potential for electrical discharge from unit when unplugged.

## 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

## Key facts

- **Recall number:** Z-2954-2026
- **Recalling firm:** SDI Limited
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-20
- **Report date:** 2026-08-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bayswater, Australia

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2954-2026

## Citation

> MORVS. FDA recall Z-2954-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2954-2026. Source: US FDA. Licensed CC0.

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