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RecallWatchMedical Device Safety
Class IIOngoingZ-2424-2026

Medline Industries, LP recalls Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB GENERA…

Medline Industries, LPNorthfield, IL, United StatesReported Jun 24, 2026 · 24 days ago
Legal News Analyst ·

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.

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB GENERAL LAPAROSCOPY PA DYNJ58305 CHRISTUS CH PEDIATRIC BASIC DYNJ61167G CVC INSERTION BUNDLE CVI3940A DAVINCI PACK SURGICOUNT DYNJ45544F EPCH BASIC PACK DYNJ83094C GENERAL PACK DYNJ39682B DYNJ84882 GENERAL RFD DYNJ906336F GENERAL SURGERY PACK DYNJT6003 GV MACD PACK DYNJ46952M IMPLANT PACK - BBI AR DYNJ63508A KIT THORACOSCOPY DYNJ908872F LVAD TRAY DM1120A MAJOR UROLOGY PACK-LF DYNJ0368525M MICRODISECT DECOMPRESS-LF DYNJ911467 MINOR PACK DYNJ86972 MULTI PURPOSE PACK DYNJ58406B OPEN HEART DYNJ903245C P&K PACK DYNJT5838 PACK,PEDIATRIC MAJOR DYNJ906888F PCNL DYNJ904468C PEDIATRIC MINOR RFD DYNJ906296I PEDIATRIC PACK DYNJ54239K PEDIATRIC SURGERY DYNJ81474B PERLMUTTER PACK DYNJT7387 RFT ISC NOBLES MINOR PACK DYNJ43954B ROBOTICS FMOL LADY OF THE LAKE DYNJ89584 ROBOTICS PACK DYNJ83622B SCOLI PACK NTX DYNJ68415C SMALL ABDOMINAL PACK-LF PHS41749G STIM IMPLANT TRIALS DYNJ87790A SUPPLEMENTAL PACK DYNJ65244 TENEX PACK DYNDH2190 THORACIC PACK DYNJ56616G THORACIC PACK SHD DYNJ68416C THORACOSCOPY DYNJ9425843R THORACOTOMY PM DYNJ906815A THORACOTOMY THORACOSCOPY DYNJ902882D TRAY,NEONATAL PICC DRSG CHANGE DYNDC1533B UNIVERSAL-ASCDYNJ900071C
    UDI-DI 10198459394577
    141 affected lots
    25JBX559DYNJ68484B1019845936896725LME889DYNJ583051088994284376325KBA708DYNJ61167G
    +133 more1019845938667125KBN90425LBQ928CVI3940A1065316099897626AME675DYNJ45544F1019348987613025KBJ042DYNJ83094C1019845956205125JMD330DYNJ39682B1019348976924125KBI41025LBI97826BBC735DYNJ848821019532743232426CBQ487DYNJ906336F1019845941995925KBR49726CBO946DYNJT60031019845953125525JBV85026CBC211DYNJ46952M1019845909013425KBH40125LBO238DYNJ63508A1019348936384526BBC181DYNJ908872F1019845966030626BBR620DM1120A1065316099889125KBA42525LBJ075DYNJ0368525M1019348982024925KBG89525KBG896DYNJ9114671019845935856225LBA393DYNJ869721019532769429626CBD230DYNJ58406B1019348995722825JBT217DYNJ903245C1088994289017026ABG614DYNJT58381019845951332925JBT808DYNJ906888F1019845919476426AMC879DYNJ904468C1019532763141325KBL838DYNJ906296I1019845941982925KBN303DYNJ54239K1019845944320625LMG373DYNJ81474B1019845910026025JBY253DYNJT73871019845961592426CBQ932DYNJ43954B1019348950916825LMI928DYNJ895841019845927872325JBS43325LBO81525LBP820DYNJ83622B1019845940273925JBA25125JBX613DYNJ68415C1019532734174925KBM18526BBD267PHS41749G1019845943884425LMG971DYNJ87790A1019845935896825KBC71825KBC975DYNJ652441019348925743425KBC47926CBC173DYNDH21901019845946796725KBE08625KBM732DYNJ56616G1019845953316725LBD70526CBC585DYNJ68416C1019532734168825KBH744DYNJ9425843R1019845908549925KMC242DYNJ906815A1019532702701826BBO802DYNJ902882D1019845949679025LBR117DYNDC1533B1088994281392625JBU460DYNJ900071C1019845912172226AMH36526AMH758

What the firm is doing

Firm began notifying consignees on 4/27/2026. Customers were instructed to request stickers to over-label affected convenience kits with a warning label. Warning label indicates for user to remove the affected component and replace it with product from supply. No kits are to be returned.

DistributionShow details

US Nationwide distribution. OUS distribution pending.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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