Use cautionMedical device recall · FDA · Published August 31, 2026
Medline Convenience Kits with AirSeal Access Ports May Cause Procedure Delays
Medline recalls 3,551 convenience kits containing AirSeal Access Ports due to potential for erroneous overpressure alerts and system venting during surgery, which may delay or end procedures.
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.
“Medline Convenience Kits with AirSeal Access Ports May Cause Procedure Delays.” GovInfoNow, updated October 27, 2026. https://govinfonow.com/recall/1764717-medline-industries-lp-recalls-convenience-kits-containing-conmed-airseal-access. Based on FDA recall #Z-0184-2027 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0184-2027%22&limit=1).
The FDA announced on Aug. 31, 2026, that Medline Industries, LP is recalling 3,551 Convenience Kits containing CONMED AirSeal Access Ports due to potential erroneous overpressure alerts and system venting during use. Owners should stop using the kits immediately.
How to tell if you have it
Brand: Medline
Product: Convenience Kits with AirSeal Access Ports
Distribution: US Nationwide in AZ, CA, IN, MD, MO, NJ, OH, and WI
The hazard
The recalled kits contain CONMED AirSeal Access Ports that may generate erroneous overpressure alerts or vent the system during use. This malfunction could result in delays or the ending of medical procedures.
Context
GovInfoNow's records show Medline Industries, LP has issued 72 other recalls since July 31, 2025. Recent Medline recalls include a Sept. 11, 2026, Foot Ankle Kit recall for shelf-life discrepancies and a Sept. 2, 2026, surgical convenience kit recall for non-conforming cannula components. Other recent recalls of similar products include ConMed AirSeal 5mm Access Port Recalls (May 14, 2026) and a ConMed AirSeal 8mm Access Port Recall (May 14, 2026).
How to tell if you have this one
Check for kits with model numbers DYNJ911135A or DYNJ906731M. These were sold nationwide in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.
Brand
Medline
Category
Medical device
FDA recall event · 6 products
All 6 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.
Look for model numbers DYNJ911135A or DYNJ906731M on the kits.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 8 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, California, Indiana, Maryland, Missouri, New Jersey, Ohio, Wisconsin.
Recall timeline
FDA published this recall 51 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0184-2027 (August 31, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0184-2027 to see it in context.
Plain-language summary written by qwen3:4b on October 27, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.