# FDA device recall: GM Helix Implant, Endosseous Dental Implant  Article No. 109.984

> recall · VERIFIED · 2026-07-13

Firm: Straumann USA LLC · Class II · There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect implant is installed, the issue could cause bon

- Company: Straumann USA LLC
- Sector: medical devices
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.