# FDA recall Z-1188-2026

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

## Product

Medline medical procedure convenience kits labeled as:    1) PACER / CATH LAB PACK-LF, Kit SKU DYNJ0972604A;   2) PACEMAKER/ICD PACK, Kit SKU DYNJ33822L;   3) VENOUS ACCESS PACK, Kit SKU DYNJ45640B;   4) PACEMAKER SET UP, Kit SKU DYNJ63377D;   5) PACK PACEMAKER CUSTOM,9909178, Kit SKU DYNJ65011D;   6) HEART BASIC OPEN PACK, Kit SKU DYNJ69143C;   7) SCC VEIN PACK, Kit SKU DYNJ69313;   8) CV PACK, Kit SKU DYNJ86007B.

## 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-1188-2026
- **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-1188-2026

## Citation

> AI Analytics. FDA recall Z-1188-2026. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-1188-2026. Source: US FDA. Licensed CC0.

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