The FDA has posted 12 enforcement recalls from ConMed Corporation since 2025, none of them Class I (most serious). Most recent report: Sep 2, 2026.
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Potential for overpressure alerts.
Firm name as filed with the FDA: “ConMed Corporation”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.