Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC… — Class II medical device recall Z-2444-2026

Ongoing recall by Medline Industries, LP, reported 2026-06-24, distributed nationwide. Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during

Recall number	`Z-2444-2026`
Product type	Medical device
Classification	Class II
Status	Ongoing
Voluntary or mandated	Voluntary
Recalling firm	Medline Industries, LP, Northfield, IL, United States
Recall initiated	2026-04-27
Classified	2026-06-12
Reported by FDA	2026-06-24
Distributed	Nationwide (US)
Quantity	49,654 kits
Reason classes	packaging
UPC / GTIN / UDI-DI	`10193489494983`, `10193489793680`, `10193489852981`, `10193489902044`, `10193489903669`, `10195327104542`, `10195327227340`, `10195327361785`, `10195327512699`, `10195327515232`, `10195327565374`, `10195327674755`, `10198459149139`, `10198459224447`, `10889942403905`
Lot numbers	`25JBW040`, `25KBC715`, `25KBG852`, `25KBH774`, `25KBI240`, `25KBK220`, `25LBB895`, `25LBO027`, `25LBP470`, `25LBQ917`, `25LMF965`, `25LMG563`, `25LMJ305`, `26ABE755`, `26BBB852`, `26CBB662`, `26CBC772`, `26CBE736`, `CDS983672P`, `CDS983686I`, `DYNJ0618174N`, `DYNJ0972604A`, `DYNJ21877W`, `DYNJ29135N`, `DYNJ35761D`, `DYNJ39316D`, `DYNJ43663A`, `DYNJ45640B`, `DYNJ52059D`, `DYNJ56573B`, `DYNJ58354F`, `DYNJ65916B`
Model numbers	`DYNJ0972604A`

Product

Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR SURGICOUNT PACK DYNJ56573B ENDOVASCULAR PACK DYNJ29135N EP DEVICE DYNJ65916B FULL LINE ANEURYSM CDS CDS983672P GEN FEM POP #14-RF DYNJ21877W IMPLANT PACK DYNJ39316D OPEN HEART MRNGSD DYNJ58354F PACEMAKER PACK-LF DYNJ0618174N PACEMAKER SETUP PACK DYNJ35761D PACER / CATH LAB PACK-LF DYNJ0972604A PACER CDS CDS983686I PACER PACK DYNJ52059D PK, EP LAB PACEMAKER DYNJ43663A VENOUS ACCESS PACK DYNJ45640B

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2444-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.