# FDA recall Z-0558-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-10-25.

## Product

ENDO KIT, Medline Kit SKU DYKE1577A, Component Number 57469, 10 per case;  Medline Convenience Kits containing Single Use Biopsy Valve MAJ-1555

## Reason for recall

Identified lots of Olympus product may be missing sterile and manufacturing lot numbers and expiration dates on the sterile packaging. The information can be found on the outer box or zipper bag label. Medline is recalling its kits which utilize affected product as a component.

## Distribution

US Nationwide distribution in the state of NY.

## Key facts

- **Recall number:** Z-0558-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-10-25
- **Report date:** 2024-12-04

- **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-0558-2025

## Citation

> AI Analytics. FDA recall Z-0558-2025. Retrieved 2026-07-28 from https://api.ai-analytics.org/recall/Z-0558-2025. Source: US FDA. Licensed CC0.

---

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