# FDA recall Z-1192-2026

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

## Product

Medline medical procedure convenience kits labeled as:    1)	MEM MAXILLOFACIAL PACK-LF, Kit SKU DYNJ0660040R;   2)	PLASTICS VCH, Kit SKU DYNJ39225K;   3)	WT BREAST PACK, Kit SKU DYNJ46620I;   4)	ENDO / AUG PACK, Kit SKU DYNJ59250I;   5)	KMC PLASTIC/GEN PACK-LF, Kit SKU DYNJ65980J;   6)	PLASTICS PACK, Kit SKU DYNJ68288A;   7)	IMPLANT REMOVAL KIT, Kit SKU MNS13035;   8)	PLASTICS PACK-LF, Kit SKU PHS41746D.

## 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-1192-2026
- **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-1192-2026

## Citation

> AI Analytics. FDA recall Z-1192-2026. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1192-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*