# FDA recall Z-2996-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-04-08.

## Product

Medline Convenience kits labeled as:    1) DIALYSIS CATHETER INSERTION KIT, Pack Number CVI4815;   2) ANGIO PACK, Pack Number CVI5045;   3) CHILDRENS INFANT SP TRAY, Pack Number DYNDA2906;   4) ULTRASOUND GUIDE BREAST BIOPSY, Pack Number DYNDH1319;   5) BIOPSY TRAY, Pack Number DYNDH1693A;   6) PACK,ULTRASOUND, Pack Number DYNDL1461;   7) LUMBAR PUNCTURE TRAY, Pack Number DYNJTS4306;   8) ARTHROGRAM TRAY, Pack Number SPEC0143A;   9) PD CATH KIT, Pack Number UVT1205

## 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.

## Key facts

- **Recall number:** Z-2996-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-08
- **Report date:** 2024-09-18

- **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-2996-2024

## Citation

> AI Analytics. FDA recall Z-2996-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2996-2024. Source: US FDA. Licensed CC0.

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