medical MODERATE Updated 2026-10-21

Medline Industries, LP recalls Convenience Kits containing CONMED AirSeal Access Ports A

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Recalled Product

Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135 LAP CHOLE DYNJ911660 LAP NISSEN DYNJ911560 UROLOGY LAPAROSCOPIC - 51638 DYNJ908720A

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: 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

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
View official government recall