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RecallsAboutBlog

ConMed Corporation

ConMed Corporation: 2 recalls listed since June 2026 across FDA.

By year

  • 20262

By agency

  • FDA2

By category

  • Medical Device2

All recalls (2)

CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver

The suture anchor may contain an incorrect patient implant card, affecting device identification and traceability.

Moderate risk, FDA, , Device defect

ConMed AirSeal Access Ports and Obturators

ConMed AirSeal Access Port and Obturator may cause overpressure alerts.

Moderate risk, FDA, , Device defect
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