- Recalling firm
- SDI Limited
- Reason for recall
- Potential for electrical discharge from unit when unplugged.
- Affected products (lot / model / serial)
- UDI:9336472005542; Serial Numbers 0003-1533
- Units affected
- 1,444 units
- Distribution pattern
- 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
- Firm location
- Bayswater, Australia
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2954-2026
- Recall initiated
- July 20, 2026
- FDA classification date
- August 14, 2026
- FDA report date
- August 26, 2026
- FDA event ID
- 99322
- Last updated on HTM Vibe
- September 8, 2026