Fresh Recalls

ConMed recalls

12 recent recalls on record for ConMed in connected official government data as of October 22, 2026 at 6:00 PM UTC.

Models with recalls

CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5 (1)ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip (1)ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip (1)ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip (1)ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip (2)ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip (1)ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip (3)ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip (2)

All ConMed recalls

FDA Class II · Medical device · September 2, 2026

CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5 recall — ConMed Corporation

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

Official ID Z-3018-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Official ID Z-2474-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Official ID Z-2473-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Official ID Z-2472-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Official ID Z-2471-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Official ID Z-2470-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Official ID Z-2469-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Official ID Z-2468-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Official ID Z-2467-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

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

Potential for overpressure alerts.

Official ID Z-2466-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

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

Potential for overpressure alerts.

Official ID Z-2465-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip recall — ConMed Corporation

Potential for overpressure alerts.

Official ID Z-2464-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.