# FDA recall Z-1196-2026

> **Medline Industries, LP** · Class II · device recall initiated 2025-12-12.

## 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.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1196-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-12
- **Report date:** 2026-02-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1196-2026

## Citation

> AI Analytics. FDA recall Z-1196-2026. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1196-2026. Source: US FDA. Licensed CC0.

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