# FDA device recall: ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS5-

> recall · VERIFIED · 2026-05-14

Firm: ConMed Corporation · Class II · Potential for overpressure alerts.

- Company: ConMed Corporation
- Sector: medtech
- 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.