This is part of a larger recall. The most authoritative record is FDA-Device / Z-0181-2027.
Medline Convenience Kits with CONMED AirSeal Access Ports recalled for erroneous pressure alerts
What this means
Medline's Convenience Kits containing CONMED AirSeal Access Ports may experience erroneous overpressure alerts and unintended system venting during laparoscopic surgical procedures. This malfunction could delay or prematurely end a procedure.
- Check if your facility received affected kits (lots 26EDA606, 25KDA658, 25KDB571, 25LDB411, or 26CDA536).
- Do not use affected kits for new procedures.
- Contact Medline Industries or your supplier for instructions on replacement or return.
The agency's original wording
Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0184-2027More Medline recalls
- FDA-Device2026-10-22Medline medical convenience kits recalled for difficult removal and adhesive residue
- FDA-Device2026-10-22Medline sterile C-section surgical drape recalled for difficult removal and skin adhesive residue
- FDA-Device2026-10-22Medline medical convenience kits recalled for difficult removal and adhesive residue
- FDA-Device2026-10-22Medline surgical convenience kits recalled for difficult removal and adhesive residue
- FDA-Device2026-10-22Medline tubal ligation surgical kit recalled for difficult removal and skin adhesive residue
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