ConMed recalls

ConMed Corporation is recalling certain lots of AirSeal 12mm Access Port and Palm Grip Obturator devices used during laparoscopic surgery. The devices may generate false overpressure alerts that could disrupt surgical procedures.

ConMed has recalled certain lots of its AirSeal 12mm Access Port with Low Profile Obturator (a surgical instrument used in minimally invasive laparoscopic procedures) due to a potential malfunction in the overpressure alert system. The affected devices may fail to properly alert during elevated pressure conditions.

ConMed has recalled certain lots of the AirSeal 12mm Access Port with Palm Grip Obturator (catalog number iAS12-150LPI), a surgical trocar used in laparoscopic procedures. The device may generate overpressure alerts during use, which could affect the surgeon's ability to maintain proper insufflation during surgery.

ConMed Corporation is recalling certain batches of the AirSeal 5mm Access Port with Low Profile Obturator (catalog number iAS5-100LP), used during laparoscopic surgery to maintain gas pressure in the abdomen. The device may generate overpressure alerts that could affect surgical workflow. No injuries have been reported.

ConMed Corporation has recalled certain lots of the AirSeal 5mm Access Port and Low Profile Obturator (catalog number iAS5-120LP), a disposable surgical trocar used in laparoscopic procedures. The device may generate overpressure alerts during use. This recall affects approximately 196,751 units distributed nationwide and internationally from June 2024 through January 2026.

ConMed has recalled certain lots of the AirSeal 5mm Access Port with Low Profile Obturator, a surgical instrument used in laparoscopic procedures. The device may generate overpressure alerts that could affect proper operation during surgery.

ConMed Corporation is recalling certain AirSeal 8mm Access Port and Low Profile Obturator devices (catalog number iAS8-100LP) used in laparoscopic surgery. The devices may generate false overpressure alerts during use. No injuries have been reported.

ConMed Corporation is recalling specific lots of its AirSeal 8mm Access Port with Low Profile Obturator (catalog number iAS8-120LP) used in laparoscopic surgery. The device may generate overpressure alerts that could affect proper operation during procedures. The recall affects approximately 55,694 packs distributed nationwide and internationally.

ConMed Corporation recalled certain AirSeal 12mm Access Ports (catalog number iASB12-100) used in laparoscopic surgery due to a potential for overpressure alerts. The affected devices were manufactured between June 2024 and January 2026, and were distributed nationwide and internationally.

ConMed Corporation is recalling certain AirSeal 12 mm Access Port and Obturator units (catalog iASB12-120) used in laparoscopic surgery because they may fail to generate proper overpressure alerts. This could allow pressure levels to rise unexpectedly during procedures. The affected units were manufactured between June 2024 and January 2026.

ConMed Corporation is recalling certain AirSeal 5mm Smooth Access Ports (Catalog Number iASB5-150) used in laparoscopic surgery. The device may generate overpressure alerts during use, which could affect surgical workflow or require device replacement during a procedure.