Medline medical procedure convenience kits labeled as: 1) DEPAUL… — Class II medical device recall Z-1196-2026

Ongoing recall by Medline Industries, LP, reported 2026-02-04, distributed nationwide. Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to c

Recall number	`Z-1196-2026`
Product type	Medical device
Classification	Class II
Status	Ongoing
Voluntary or mandated	Voluntary
Recalling firm	Medline Industries, LP, Northfield, IL, United States
Recall initiated	2025-12-12
Classified	2026-01-28
Reported by FDA	2026-02-04
Distributed	Nationwide (US)
Quantity	236 units
Reason classes	packaging
UPC / GTIN / UDI-DI	`10198459228995`, `10198459231339`, `10198459443138`, `10198459495427`, `10198459526404`, `10198459553660`, `40198459228996`, `40198459231330`, `40198459443139`, `40198459495428`, `40198459526405`, `40198459553661`
Lot numbers	`25JDB033`, `25KMC287`, `25KMD463`, `25KMD804`, `25KMH940`, `25LMA824`

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 for recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1196-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.