ConMed Corporation Recalls

12 recalls on record in the United States

medical: 12
medical Class II
2026-06-24

ConMed Corporation recalls ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip

Potential for overpressure alerts.

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medical Class II
2026-06-24

ConMed Corporation recalls ConMed AirSeal 5mm Access Port and Low Profile Obturator wit

Potential for overpressure alerts.

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medical Class II
2026-06-24

ConMed Corporation recalls ConMed AirSeal 12mm Access Port and Low Profile Obturator wi

Potential for overpressure alerts.

View recall details →

medical Class II
2026-06-24

ConMed Corporation recalls ConMed AirSeal 5 mm Smooth Access Port and Obturator with Bl

Potential for overpressure alerts.

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medical Class II
2026-06-24

ConMed Corporation recalls ConMed AirSeal 8mm Access Port and Low Profile Obturator wit

Potential for overpressure alerts.

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medical Class II
2026-06-24

ConMed Corporation recalls ConMed AirSeal 8mm Access Port and Low Profile Obturator wit

Potential for overpressure alerts.

View recall details →

medical Class II
2026-06-24

ConMed Corporation recalls ConMed AirSeal 12mm Access Port and Palm Grip Obturator with

Potential for overpressure alerts.

View recall details →

medical Class II
2026-06-24

ConMed Corporation recalls ConMed AirSeal 5mm Access Port and Low Profile Obturator wit

Potential for overpressure alerts.

View recall details →

medical Class II
2026-06-24

ConMed Corporation recalls ConMed AirSeal 5mm Access Port and Low Profile Obturator wit

Potential for overpressure alerts.

View recall details →

medical Class II
2026-06-24

ConMed Corporation recalls ConMed AirSeal 12 mm Access Port and Obturator with Blunt Ti

Potential for overpressure alerts.

View recall details →

medical Class II
2026-06-24

ConMed Corporation recalls ConMed AirSeal 12mm Access Port and Palm Grip Obturator with

Potential for overpressure alerts.

View recall details →

medical Class II
2026-09-02

ConMed Corporation recalls CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposabl

Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.

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