# FDA recall Z-1464-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2025-02-11.

## Product

Medline procedure kits labeled as:    1) ACOUSTIC NEUROMA PACK-LF, Pack Number DYNJ37741B;   2) ANGIOGRAPHY PACK, Pack Number DYNJ21519W;   3) NEURO ANGIO PACK, Pack Number DYNJ83941;   4) NEURO ANGIO PACK SJF-LF, Pack Number DYNJ55678;   5) NEURO PACK, Pack Number DYNJ04851Q;   6) SNI NEURO, Pack Number DYNJ45379D;   7) VP SHUNT PACK, Pack Number DYNJ55558C

## Reason for recall

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.

## Distribution

Worldwide distribution - US Nationwide and the country of Canada.

## Key facts

- **Recall number:** Z-1464-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-11
- **Report date:** 2025-04-02

- **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-1464-2025

## Citation

> AI Analytics. FDA recall Z-1464-2025. Retrieved 2026-07-07 from https://api.ai-analytics.org/recall/Z-1464-2025. Source: US FDA. Licensed CC0.

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