FDA-Device2026-10-21Class IIPROCESSING DEFECT

Medline Convenience Kits with CONMED AirSeal Access Ports recalled for erroneous pressure alerts

OTHERNationwide distributionMedical devices

What this means

Medline Industries Convenience Kits containing CONMED AirSeal Access Ports may experience erroneous overpressure alerts and unintended system venting during surgical procedures. This defect could cause delays or premature termination of procedures.

  • Check if you have one of the affected kits (model numbers DYNJG901004C, DYNJ88071, or DYNJ50474F) by looking at lot numbers listed in this recall.
  • Contact Medline Industries or your surgical facility for instructions on device replacement or repair.
  • Report any problems with the device to the FDA MedWatch program.
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The agency's original wording
Hazard

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.

Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.
Affected count
3,551 kits
Manufactured in
3 Lakes Dr, Northfield, IL, United States
Products
Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI DYNJG901004C LAP CHOLE DYNJ88071 ROBOTIC PACK DYNJ50474F

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0182-2027

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