Medline Industries recalls

Medline Industries has 705 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 30 Sep 2026. 537 are still ongoing. 525 were reported in the last 12 months.

Total recalls705since 2012
Last 12 months525reported
Class I9614% of total
Ongoing537latest 30 Sep 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 96 14%Class II 606 86%Class III 3 0%

Why medline industries is recalled

By year

Ongoing medline industries recalls

537 active

All medline industries recalls, newest first

705 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIMedline Convenience Kits: Major Pack recalled by Medline IndustriesMedline IndustriesOtherNationwide
DeviceCLASS IIMedline Convenience Kits: Peds Sinus Pack recalled by Medline IndustriesMedline IndustriesOtherNationwide
DeviceCLASS IIMedline Convenience Kits: Mfc Craniotomy Pack recalledMedline IndustriesOtherNationwide
DeviceCLASS IIMedline convenience kits containing Healthmark Instrument recalledMedline IndustriesOtherNationwide
DeviceCLASS IIMedline Convenience Kits: Major Neuro Vch recalled by Medline IndustriesMedline IndustriesOtherNationwide
DeviceCLASS IIMedline Convenience Kits: Anterior Spine Pack recalledMedline IndustriesOtherNationwide
DeviceCLASS IIMedline convenience kits containing Healthmark Instrument recalledMedline IndustriesOtherNationwide
DeviceCLASS IIConvenience kits Cataract Pack DYNJ59881A recalled by Medline IndustriesMedline IndustriesSterilityNationwide
DeviceCLASS IMedline Convenience Kits: Port Access Kit Univ OF Ala recalledMedline IndustriesSterilityNationwide
DeviceCLASS IIConvenience kits Minor Pack DYNJ58421A Springhill Minor recalledMedline IndustriesSterilityNationwide
DeviceCLASS IMedline Convenience Kits recalled by Medline IndustriesMedline IndustriesSterilityNationwide
DeviceCLASS IIConvenience kits Anesthesia Pain PK League DYNJ67925A recalledMedline IndustriesSterilityNationwide
DeviceCLASS IIConvenience kits Myringotomy Pack-lf DYNJ59097A recalledMedline IndustriesSterilityNationwide
DeviceCLASS IMedline Convenience Kits recalled by Medline IndustriesMedline IndustriesSterilityNationwide
DeviceCLASS IMedline Convenience Kits: Open Heart Adult recalledMedline IndustriesSterilityNationwide
DeviceCLASS IMedline Convenience Kits recalled by Medline IndustriesMedline IndustriesSterilityNationwide
DeviceCLASS IMedline Convenience Kits: Kit Anesthesia L&d A- Line Set recalledMedline IndustriesSterilityNationwide
DeviceCLASS IIMedline Convenience Kit: Open Heart A Pack recalledMedline IndustriesSterilityNationwide
DeviceCLASS IMedline Convenience Kits recalled by Medline IndustriesMedline IndustriesSterilityNationwide
DeviceCLASS IIMedline Convenience Kits: Blood Draw Kit recalled by Medline IndustriesMedline IndustriesSterilityNationwide
DeviceCLASS IIMedline Convenience Kits containing BD ChloraPrep Clear recalledMedline IndustriesPackaging DefectsNationwide
DeviceCLASS IIMedline Convenience Kits: Ortho Aspiration Kit recalledMedline IndustriesSterilityNationwide
DeviceCLASS IIMedline Convenience Kits containing BD ChloraPrep DYKA1054F recalledMedline IndustriesPackaging DefectsNationwide
DeviceCLASS IIMedline Convenience Kits: Arterial Line Insertion Kit recalledMedline IndustriesSterilityNationwide
DeviceCLASS IIMedline Convenience Kits containing BD ChloraPrep Clear recalledMedline IndustriesPackaging DefectsNationwide
DeviceCLASS IIMedline Convenience Kits: Colorectal ME recalled by Medline IndustriesMedline IndustriesSterilityNationwide
DeviceCLASS IIMedline Convenience Kits containing BD ChloraPrep Clear recalledMedline IndustriesPackaging DefectsNationwide
DeviceCLASS IIMedline Convenience Kits containing BD ChloraPrep Clear recalledMedline IndustriesPackaging DefectsNationwide
DeviceCLASS IIMedline Convenience Kits containing BD ChloraPrep Clear recalledMedline IndustriesPackaging DefectsNationwide
DeviceCLASS IIMedline Convenience Kits: Pre-op KIT recalled by Medline IndustriesMedline IndustriesSterilityNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.