# FDA recall Z-3041-2024

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

## Product

Medline Convenience kits labeled as:    1) CHEST TUBE INSERTION TRAY, Pack Number DYNDA2063;   2) PULL D/C PACK, Pack Number DYNDA2080;   3) STERILE 3CC SYR W/ 23GX1 NDL, Pack Number DYNDA2495;   4) STERILE 1CC SYR W/ 25GX5/8 NDL, Pack Number DYNDA2497;   5) ARTHROGRAM TRAY, Pack Number DYNDH1113;   6) ARTHROGRAM TRAY, Pack Number DYNDH1134;   7) BIOPSY TRAY, Pack Number DYNDH1137C;   8) BREAST BIOPSY TRAY, Pack Number DYNDH1257;   9) OHS CT BIOPSY TRAY -LF, Pack Number DYNDH1270;   10) LUMBAR PUNCTURE TRAY, Pack Number DYNDH1275;   11) ISHAK I.R. BIOPSY TRAY, Pack Number DYNDH1297;   12) ISHAK IR DRAINAGE TRAY, Pack Number DYNDH1300;   13) ULTRASOUND GUIDE BREAST BIOPSY, Pack Number DYNDH1319;   14) LUMBAR PUNCTURE TRAY, Pack Number DYNDH1321;   15) MINI INTERVENTIONAL PACK, Pack Number DYNDH1324B;   16) DIAGNOSTIC TRAY, Pack Number DYNDH1359;   17) LUMBAR TRAY, Pack Number DYNDH1500;   18) TRAY SAFETY LUMBAR PUNCTURE 18GX3.5, Pack Number DYNDH1538;   19) TRAY SAFETY LUMBAR PUNCTURE 2

## 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-3041-2024
- **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-3041-2024

## Citation

> AI Analytics. FDA recall Z-3041-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-3041-2024. Source: US FDA. Licensed CC0.

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