CLASS II ONGOING Device recall · Reported 24 Jun 2026 · FDA Enforcement Report

Medline convenience kits: Davinci DYNJ905836D Davinci-lf recalled

Medline Industries is recalling Medline convenience kits: Davinci DYNJ905836D Davinci-lf DYNJ905293I General Robotics, distributed nationwide in the US. The recall was initiated on 27 Apr 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesDYNJ905836D UDI-DI 10195327517977 Lot 25LBB534 DYNJ905293I UDI-DI 10198459247972 Lot 25KBM585 DYNJT8308 UDI-DI 10198459697135 Lot 26CBD040 CDS860087Q UDI-DI 10198459543005 Lots 25JBV094 25LBP061 DYNJ910084C UDI-DI 10198459597466 Lot 25LBE810 CDS982371I UDI-DI 10198459044106 Lots 25KBH343 26CBN241 CDS920099S UDI-DI 10195327140656 Lot 25KBO172 DYNJT3887 UDI-DI 10198459366871 Lot 25JBX564 DYNJT6876 UDI-DI 10198459583148 Lot 25KBM646 CDS984228K UDI-DI 10198459044113 Lot 26ABF608 DYNJ911843 UDI-DI 10198459555206 Lot 25LBC203 DYKMBNDL165C UDI-DI 10198459634284 Lot 25LBR024 CDS985442J UDI-DI 10198459476686 Lot 25JBT926 DYNJ84725B UDI-DI 10198459366949 Lot 25JBA329 DYNJ910594B UDI-DI 10198459563768 Lot 25KBJ104 DYNJ53711B UDI-DI 10198459023538 Lots 25KBF929 25LBB875 DYNJ83622C UDI-DI 10198459607172 Lots 25LBR740 26CBJ460 DYNJ909322B UDI-DI 10198459443848 Lot 25LBD961 DYNJ902583O UDI-DI 10198459441806 Lot 25LBC041
Quantity recalled49,654 kits total

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-2431-2026
FDA event ID
98951
Recalling firm
Medline Industries, Northfield, IL
Classification
Class II
Status
Ongoing
Recall initiated
27 Apr 2026
FDA classified
12 Jun 2026
Reported
24 Jun 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Device Malfunction

Timeline

27 Apr 2026Recall initiated by company
12 Jun 2026Classified by FDA+46 days
24 Jun 2026Published in enforcement report+12 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 recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.

Product as listed by the FDA

Medline convenience kits: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I GENERAL ROBOTICS PACK DYNJT8308 GYN LAP CDS860087Q GYN LAPAROSCOPY DYNJ910084C GYN LAPAROSCOPY CDS CDS982371I GYN LAPAROSCOPY CDS #34-RF CDS920099S GYN LAPAROSCOPY PACK DYNJT3887 DYNJT6876 GYN ROBOTIC CDS CDS984228K GYN ROBOTICS DYNJ911843 KIT LABOR DELIVERY TUBAL LIGAT DYKMBNDL165C ROBOTIC LAP CHOLE CDS CDS985442J ROBOTIC PACK DYNJ84725B DYNJ910594B ROBOTIC SURGERY PACK DYNJ53711B ROBOTICS PACK DYNJ83622C UOFL GYN LAPAROSCOPY DYNJ909322B WMC ROBOTIC PACK - LF DYNJ902583O

Where it was distributed

US Nationwide distribution. OUS distribution pending.

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

DYNJ905836D UDI-DI 10195327517977 Lot 25LBB534 DYNJ905293I UDI-DI 10198459247972 Lot 25KBM585 DYNJT8308 UDI-DI 10198459697135 Lot 26CBD040 CDS860087Q UDI-DI 10198459543005 Lots 25JBV094 25LBP061 DYNJ910084C UDI-DI 10198459597466 Lot 25LBE810 CDS982371I UDI-DI 10198459044106 Lots 25KBH343 26CBN241 CDS920099S UDI-DI 10195327140656 Lot 25KBO172 DYNJT3887 UDI-DI 10198459366871 Lot 25JBX564 DYNJT6876 UDI-DI 10198459583148 Lot 25KBM646 CDS984228K UDI-DI 10198459044113 Lot 26ABF608 DYNJ911843 UDI-DI 10198459555206 Lot 25LBC203 DYKMBNDL165C UDI-DI 10198459634284 Lot 25LBR024 CDS985442J UDI-DI 10198459476686 Lot 25JBT926 DYNJ84725B UDI-DI 10198459366949 Lot 25JBA329 DYNJ910594B UDI-DI 10198459563768 Lot 25KBJ104 DYNJ53711B UDI-DI 10198459023538 Lots 25KBF929 25LBB875 DYNJ83622C UDI-DI 10198459607172 Lots 25LBR740 26CBJ460 DYNJ909322B UDI-DI 10198459443848 Lot 25LBD961 DYNJ902583O UDI-DI 10198459441806 Lot 25LBC041

Where was it sold?

US Nationwide distribution. OUS distribution pending.

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 26 Sep 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

33 other products · FDA event 98951

This product is part of a recall event; the main page for the event is Medline convenience kits: Cmh Central Line Dressing Change recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IIMedline convenience kits: Cmh Central Line Dressing Change recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Davinci Main DYNJ908031D recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Acd DYNJ904999J Acdf DYNJ907336B recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIBlock Tray Dynjra2119a Indwelling Nerve Block Dynjra1011a recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: WT Lavh Pack DYNJ46609F recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kit: Smsc-pelviscopy Pack-lf DYNJ0161619M recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kit: Hernia Repair Tote DYNJ908337D recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMinor Cath Lab Pack Dynj84775a Or Vascular Angio Pack recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kit: Labor & Delivery C-section DYNJ907895F recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline EBSI Kit EBSI1534 recalled by Medline IndustriesMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: C-section Kit DYNJ904305J recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Driveline Management Kit EBSI1688 recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Breast-hernia-port Cds-lf CDS984853L recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716 recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Add-a-cath Arterial Insertion recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Bib AV Fistula Pack DYNJ58304B recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Hysterectomy Pack-lf DYNJ20485L recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Breast Imaging DYNJT5893 Chog recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Inpatient Central LN Drsg Kit recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: C Section CDS985505G C Section recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Basic DYNJ905869G Basic Pack recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kit: IV Start Kit W/Hubguard DYNDV2662 recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Femoral Block Tray DYNJRA1739B recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IICenturion convenience kits: Central Line Dressing SV43 Fcp recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Abd Pack DYNJ81673B Bariatric recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kit: Bhs Neuro DYNJ904900N Medtrx Neuro recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Acl Pack DYNJ64161C Arthroscopy recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Discectomy Pack DYNJ86476B Ear recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kit: Kit: Dressing Change Ped DYNDC3359 recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Basic Eye DYNJ905154I Tubal recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: CVC Insertion KIT ECVC6805B recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Loop Pack DYNJ61460C Open Heart recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Port A Cath DYNJ906818A recalledMedline IndustriesDevice MalfunctionNationwide

More recalls from Medline Industries

All 707
ReportedClassRecallCompanyReasonWhere
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DeviceCLASS IIExpressaire Disposable Tourniquet Cuff, 12" X 3.5" 1-Line (CS Plum recalledASP GlobalDevice MalfunctionNationwide
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