Medline Industries, LP recalls See RES for complete list. Medline Convenience Kits: 1) DRAWER 6-IV FLUIDS GLOVES

Recalling company

Medline Industries, LP

Product

See RES for complete list. Medline Convenience Kits: 1) DRAWER 6-IV FLUIDS GLOVES, Model Number: ACC010326; 2) DRAWER 6-IV FLUIDS GLOVES, Model Number: ACC010326A; 3) DRAWER 6-IV FLUIDS GLOVES, Model Number: ACC010326B; 4) DRAWER #5, Model Number: ACC010475; 5) DRAWER 1 NEURO CART, Model Number: ACC010542; 6) DRAWER 2 NEURO CART, Model Number: ACC010543; 7) DRAWER 4, Model Number: ACC010722; 8) SUCTION TRAY, Model Number: ACC010862; 9) MALIGNANT HYPERTHERMIA CART, Model Number: ACC010896;

Reason

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

Classification

Class II – may cause temporary or medically reversible health consequences

Recall date

Jan 7, 2026

Reported

May 13, 2026

Distribution

Worldwide - US Nationwide distribution.

Status

Ongoing

Quantity

207196 units

Lot / codes

1) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case), Lot Number: 21CDB175; 2) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case), Lot Number: 21CDB692; 3) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case), Lot Number: 21LDA438; 4) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case), Lot Number: 22BDB172; 5) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case), Lot Number: 22HDA973; 6) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case), Lot Number: 23ADA426; 7) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case), Lot Number: 23BDA230; 8) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case), Lot Number: 23CDC052; 9) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case), Lot Number: 23CDA732; 10) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case), Lot Number: 23IDB293; 11) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case), Lot Number: 23LDB309; 12) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case), Lot Number: 23LDB516; 13) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case), Lot Number: 24ADA088; 14) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case), Lot Number: 24ADA521; 15) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case), Lot Number: 24ADB169; 16) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case), Lot Number: 24EDB837; 17) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case), Lot Numbe

Company location

Northfield, IL

Recall type

Voluntary: Firm initiated

Recall number

Z-2101-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2101-2026 in the FDA Enforcement Report. Also see FDA recall press releases.