# FDA recall Z-1189-2026

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

## Product

Medline medical procedure convenience kits labeled as:    1) BREAST-HERNIA-PORT CDS-LF, Kit SKU CDS984853L;   2) BREAST BIOPSY PACK, Kit SKU DYNJ45641B;   3) DERMATOLOGY PACK, Kit SKU DYNJT3658A.

## 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-1189-2026
- **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-1189-2026

## Citation

> AI Analytics. FDA recall Z-1189-2026. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1189-2026. Source: US FDA. Licensed CC0.

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