RecallRadar

FDA Device recall Z-0180-2027

Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135 LAP CHOLE DYNJ911660 LAP NISSEN DYNJ911560 UROLOGY…

On 2026-10-21 the FDA classified a Class II recall of Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135 LAP CHOLE DYNJ911660 LAP NISSEN DYNJ911560 UROLOGY… 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-0180-2027
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 DYNJ911135 LAP CHOLE DYNJ911660 LAP NISSEN DYNJ911560 UROLOGY LAPAROSCOPIC - 51638 DYNJ908720A

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_info
DYNJ911135 UDI-DI 10198459264382 Lots 25EDA279 25FDB612 25LDB658 DYNJ911660 UDI-DI 10198459487071 Lo…DYNJ911135 UDI-DI 10198459264382 Lots 25EDA279 25FDB612 25LDB658 DYNJ911660 UDI-DI 10198459487071 Lots 25IMF444 25JMA458 26BMG519 26DMA914 26EMA779 26FME775 26GMA849 26GMF826 26GMM101 26GMM127 DYNJ911560 UDI-DI 10198459400261 Lots 25HMG749 25JMC886 25KMA383 25KMA392 DYNJ908720A UDI-DI 10195327423155 Lots 24DBN292 24GBJ114 24IBK504 24JBC471 25KBP733 26ABG732

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-0180-2027%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.