# FDA recall Z-1709-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2025-03-19.

## Product

Medline procedure kits, labeled as:    1) STERILE PREP KIT, REF DYNDA1359A;   2) STRL EK SINGLE PACK, REF DYNDA1360B;   3) SHEATH REMOVAL TRAY, REF DYNDC1311C;   4) SENSITIVE SKIN WEEKLY VAD, REF DYNDC3185;   5) NURSING SKILLS, REF EDUC05015A;   6) NURSING SUPPLY BAG, REF EDUC1024A.

## Reason for recall

It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.

## Distribution

Worldwide distribution - US Nationwide and the countries of Panama and Canada.

## Key facts

- **Recall number:** Z-1709-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-19
- **Report date:** 2025-05-07

- **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-1709-2025

## Citation

> AI Analytics. FDA recall Z-1709-2025. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1709-2025. Source: US FDA. Licensed CC0.

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