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FDA Device recall Z-0184-2027

Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M

On 2026-10-21 the FDA classified a Class II recall of Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M by Medline Industries, citing 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 resul….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0184-2027
ClassificationClass II
Statusongoing
Initiated2026-08-31
Published2026-10-21
Last updated2026-10-27 05:30 UTC
CompanyMedline Industries
DistributionUS

Product

Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M

Reason

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.

Identifiers

code_infoDYNJ911135A UDI-DI 10198459655623 Lot 26EDA606 DYNJ906731M UDI-DI 10198459567117 Lots 25KDA658 25KDB571 25LDB411 26CDA536

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-10-27 05:30 UTC. Current status: ongoing.

Other recalls by Medline Industries

All Medline Industries recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0184-2027%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.