- Recalling firm
- Stryker Corporation
- Reason for recall
- There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
- Affected products (lot / model / serial)
- GTIN 0761332706146, Batch Numbers: 24297FG2, 24306FG2, 24344FG2, 25007FG2, 25065FG2, 25091FG2, 25168FG2.
- Units affected
- 589 Units
- Distribution pattern
- Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Chile, France, Germany, Indonesia, Italy, Mexico, Netherlands, New Zealand, Philippines, South Korea, Spain, Sweden, Switzerland, Taiwan, United Kingdom.
- Firm location
- San Jose, CA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2866-2026
- Recall initiated
- June 8, 2026
- FDA classification date
- August 3, 2026
- FDA report date
- August 12, 2026
- FDA event ID
- 99340
- Last updated on HTM Vibe
- August 18, 2026