Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC NEURO-LF

Recalling company

Medline Industries, LP

Product

Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC NEURO-LF, Kit SKU DYNJ20028L; 2) NEURO MINOR PACK, Kit SKU DYNJ46546M; 3) NEURO SHUNT PACK, Kit SKU DYNJ54396K; 4) NEURO PACK, Kit SKU DYNJ59397Q; 5) NEURO BASIC, Kit SKU DYNJ904052L; 6) PK NEURO SHUNT BUMC, Kit SKU DYNJT6428.

Reason

Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.

Classification

Class II – may cause temporary or medically reversible health consequences

Recall date

Dec 12, 2025

Reported

Feb 4, 2026

Distribution

US Nationwide distribution.

Status

Ongoing

Quantity

236 units

Lot / codes

Medline Kit SKU DYNJ20028L: UDI/DI 10198459228995 (EA) 40198459228996 (CS), Lot Number 25LMA824; Medline Kit SKU DYNJ46546M: UDI/DI 10198459526404 (EA) 40198459526405 (CS), Lot Number 25KMH940; Medline Kit SKU DYNJ54396K: UDI/DI 10198459443138 (EA) 40198459443139 (CS), Lot Number 25KMD804; Medline Kit SKU DYNJ59397Q: UDI/DI 10198459495427 (EA) 40198459495428 (CS), Lot Number 25KMC287; Medline Kit SKU DYNJ904052L: UDI/DI 10198459231339 (EA) 40198459231330 (CS), Lot Number 25JDB033; Medline Kit SKU DYNJT6428: UDI/DI 10198459553660 (EA) 40198459553661 (CS), Lot Number 25KMD463.

Company location

Northfield, IL

Recall type

Voluntary: Firm initiated

Recall number

Z-1196-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-1196-2026 in the FDA Enforcement Report. Also see FDA recall press releases.