CLASS II ONGOING Device recall · Reported 21 Oct 2026 · FDA Enforcement Report

Convenience Kits containing Conmed AirSeal Access Ports Chn recalled

Medline Industries is recalling Convenience Kits containing Conmed AirSeal Access Ports Chn Gyn Oncology DYNJ906731K, distributed nationwide in the US. The recall was initiated on 31 Aug 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesDYNJ906731K UDI-DI 10195327436346 Lots 24ADB566 24CDB291 24CDB969 24GDB449 24JDA590 24KDB303 25BDB494 25CDA446 25EDB457 25FDA837 25FDB582 25GDA082 DYNJ906731L UDI-DI 10198459403675 Lots 25HDB211 25JDA226 DYNJ906731N UDI-DI 10198459758249 Lots 26EDA043 26FDB001 26FDB487 DYNJG901002A UDI-DI 10195327401481 Lot 24BLA300 DYNJG901002B UDI-DI 10195327677145 Lots 24GLA290 24ILA519 24JLA479 24LLA939 25ALA154 25ELA210 25FLA112 25GLA399 25HLA560 DYNJG901002C UDI-DI 10198459545672 Lots 25JLA619 25KLA897 26ALA207 26BLA625 26CLA984 DYNJG901002D UDI-DI 10198459723742 Lots 26ELA161 26ELA744 26GLA765 26HLA179 DYNJG901004B UDI-DI 10195327677138 Lots 24FLA735 24GLA836 24KLA502 25ALA409 25ALA837 25DLA322 25ELA451 25FLA291 25GLB051 25HLA207 25ILA840 25JLA027 25JLA621 DYNJG901004D UDI-DI 10198459723759 Lots 26DLA382 26ELA743 26FLB123 DYNJ911258A UDI-DI 10198459582097 Lot 26AMF842 DYKMBNDL116D UDI-DI 10195327608866 Lots 24CBF889 24DBA349 DYKMBNDL116F UDI-DI 10198459000706 Lots 24DBS388 24FBC411 24GBK948 24IBV184 24JBB328 DYNJ907827F UDI-DI 10195327345365 Lots 24ABV361 24CBM651 24DBD866 24GBH678 DYNJ50474G UDI-DI 10198459140235 Lots 24KDA630 25ADB023 25BDB826 25CDB231 25DDA066 25HDA254 25JDA520 25LDA008 25LDC029 26DDA900 26FDA459 26FDB573 DYNJ63392C UDI-DI 10195327634643 Lots 24BLA318 24CLA990 24ELA575 24FLA977 24HLA137 24ILA935 DYNJ63392F UDI-DI 10198459315572 Lots 25DLA944 25ELA626 25FLA272 25GLA905 25HLA240 25HLA894 25JLA091 25KLA775 25LLA985 26ALA670 26DLB121 26FLA701

Quantity recalled3,551 kits

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0183-2027
FDA event ID: 99888
Recalling firm: Medline Industries, Northfield, IL
Classification: Class II
Status: Ongoing
Recall initiated: 31 Aug 2026
FDA classified: 15 Oct 2026
Reported: 21 Oct 2026
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Packaging Defects
Device type: Other Medical Devices

Timeline

31 Aug 2026	Recall initiated by company
15 Oct 2026	Classified by FDA	+45 days
21 Oct 2026	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

Convenience Kits containing CONMED AirSeal Access Ports CHN GYN ONCOLOGY DYNJ906731K DYNJ906731L DYNJ906731N DAVINCI PROSTATECTOMY DYNJG901002A DYNJG901002B DYNJG901002C DYNJG901002D GENERAL DAVINCI DYNJG901004B DYNJG901004D HERNANDEZ DAVINCI ACC BUNDLE M DYNJ911258A KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116D DYKMBNDL116F ROBOTIC GYN DYNJ907827F ROBOTIC PACK DYNJ50474G RR-DAVINCI PROSTATE ACCESSORY DYNJ63392C DYNJ63392F

Where it was distributed

US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.

Nationwide Arizona California Indiana Maryland Missouri New Jersey Ohio Wisconsin

Questions about this recall

Why was it recalled?

Which lots are affected?

DYNJ906731K UDI-DI 10195327436346 Lots 24ADB566 24CDB291 24CDB969 24GDB449 24JDA590 24KDB303 25BDB494 25CDA446 25EDB457 25FDA837 25FDB582 25GDA082 DYNJ906731L UDI-DI 10198459403675 Lots 25HDB211 25JDA226 DYNJ906731N UDI-DI 10198459758249 Lots 26EDA043 26FDB001 26FDB487 DYNJG901002A UDI-DI 10195327401481 Lot 24BLA300 DYNJG901002B UDI-DI 10195327677145 Lots 24GLA290 24ILA519 24JLA479 24LLA939 25ALA154 25ELA210 25FLA112 25GLA399 25HLA560 DYNJG901002C UDI-DI 10198459545672 Lots 25JLA619 25KLA897 26ALA207 26BLA625 26CLA984 DYNJG901002D UDI-DI 10198459723742 Lots 26ELA161 26ELA744 26GLA765 26HLA179 DYNJG901004B UDI-DI 10195327677138 Lots 24FLA735 24GLA836 24KLA502 25ALA409 25ALA837 25DLA322 25ELA451 25FLA291 25GLB051 25HLA207 25ILA840 25JLA027 25JLA621 DYNJG901004D UDI-DI 10198459723759 Lots 26DLA382 26ELA743 26FLB123 DYNJ911258A UDI-DI 10198459582097 Lot 26AMF842 DYKMBNDL116D UDI-DI 10195327608866 Lots 24CBF889 24DBA349 DYKMBNDL116F UDI-DI 10198459000706 Lots 24DBS388 24FBC411 24GBK948 24IBV184 24JBB328 DYNJ907827F UDI-DI 10195327345365 Lots 24ABV361 24CBM651 24DBD866 24GBH678 DYNJ50474G UDI-DI 10198459140235 Lots 24KDA630 25ADB023 25BDB826 25CDB231 25DDA066 25HDA254 25JDA520 25LDA008 25LDC029 26DDA900 26FDA459 26FDB573 DYNJ63392C UDI-DI 10195327634643 Lots 24BLA318 24CLA990 24ELA575 24FLA977 24HLA137 24ILA935 DYNJ63392F UDI-DI 10198459315572 Lots 25DLA944 25ELA626 25FLA272 25GLA905 25HLA240 25HLA894 25JLA091 25KLA775 25LLA985 26ALA670 26DLB121 26FLA701

Where was it sold?

US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 27 Oct 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

5 other products · FDA event 99888

This product is part of a recall event; the main page for the event is Convenience Kits containing Conmed AirSeal Access Ports recalled.

Reported	Class	Recall	Company	Reason	Where
21 Oct 2026	CLASS II	Convenience Kits containing Conmed AirSeal Access Ports recalled	Medline Industries	Packaging Defects	Nationwide
21 Oct 2026	CLASS II	Convenience Kits containing Conmed AirSeal Access Ports Kit recalled	Medline Industries	Packaging Defects	Nationwide
21 Oct 2026	CLASS II	Convenience Kits containing Conmed AirSeal Access Ports recalled	Medline Industries	Packaging Defects	Nationwide
21 Oct 2026	CLASS II	Convenience Kits containing Conmed AirSeal Access Ports recalled	Medline Industries	Packaging Defects	Nationwide
21 Oct 2026	CLASS II	Convenience Kits containing Conmed AirSeal Access Ports recalled	Medline Industries	Packaging Defects	Nationwide

More recalls from Medline Industries

All 726

Reported	Class	Recall	Company	Reason	Where
21 Oct 2026Device	CLASS II	Medline surgical convenience kits labeled as: EAR recalled	Medline Industries	Packaging Defects	Nationwide
21 Oct 2026Device	CLASS II	Convenience Kits containing Conmed AirSeal Access Ports recalled	Medline Industries	Packaging Defects	Nationwide
21 Oct 2026Device	CLASS II	Medline surgical convenience kits labeled as recalled	Medline Industries	Packaging Defects	Nationwide
21 Oct 2026Device	CLASS II	Convenience Kits containing Conmed AirSeal Access Ports recalled	Medline Industries	Packaging Defects	Nationwide
21 Oct 2026Device	CLASS II	Convenience Kits containing Conmed AirSeal Access Ports recalled	Medline Industries	Packaging Defects	Nationwide

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