- Recalling firm
- Boston Scientific Neuromodulation Corporation
- Reason for recall
- Sterile anchors my lack sterility assurance.
- Affected products (lot / model / serial)
- GTIN: 08714729905318/Lot # 35107836
- Units affected
- 43 units
- Distribution pattern
- US Nationwide distribution in the states of MD, UT, FL, LA, SC, OK.
- Firm location
- Valencia, CA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- N/A
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2404-2026
- Recall initiated
- April 29, 2026
- FDA classification date
- June 11, 2026
- FDA report date
- June 17, 2026
- FDA event ID
- 98941
- Last updated on HTM Vibe
- July 23, 2026