# FDA recall Z-3027-2024

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

## Product

Medline Convenience kits labeled as:    1) 6" FEMORAL ARTERIAL LINE KIT- ICU, Pack Number ART245C;   2) CHEST TUBE INSERTION TRAY, Pack Number CHT1900;   3) CHEST TUBE INSERTION TRAY, Pack Number CHT560;   4) CHEST TUBE INSERTION TRAY, Pack Number CHT705;   5) PORT TRAY , Pack Number DT19245;   6) BIOPSY KIT, Pack Number DYNDA1466A;   7) BIOPSY KIT, Pack Number DYNDA1466A;   8) CATH REMOVAL, Pack Number DYNDA1733B;   9) CATH REMOVAL, Pack Number DYNDA1814;   10) CATH REMOVAL, Pack Number DYNDA1814;   11) CATH REMOVAL, Pack Number DYNDA1814;   12) CATH REMOVAL, Pack Number DYNDA1814;   13) CATH REMOVAL, Pack Number DYNDA1814;   14) CATH REMOVAL, Pack Number DYNDA1814;   15) CATH REMOVAL, Pack Number DYNDA1814;   16) CATH REMOVAL, Pack Number DYNDA1814;   17) SHUNT TRAY, Pack Number DYNDA2725;   18) PORT ACCESS KIT, Pack Number DYNDC2945;   19) PORT ACCESS KIT, Pack Number DYNDC2945;   20) PORT ACCESS KIT, Pack Number DYNDC2945;   21) PORT ACCESS KIT, Pack Number DYNDC2945;   22) PORT AC

## 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-3027-2024
- **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-3027-2024

## Citation

> AI Analytics. FDA recall Z-3027-2024. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-3027-2024. Source: US FDA. Licensed CC0.

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