# FDA recall Z-3020-2024

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

## Product

Medline Convenience kits labeled as:   1) PRESSURE TUBING B.I., Pack Number 81239;  2) M1S1109 TRADITIONAL PROCESS-LF, Pack Number 946279 ;  3) 20GX6" FEMORAL ART LINE KIT, Pack Number ART1165;  4) 3" RADIAL ARTERIAL LINE KIT- OR, Pack Number ART1210;  5) 3" RADIAL ARTERIAL LINE KIT- ICU, Pack Number ART240B;  6) 18GX6" FEMORAL ART LINE KIT, Pack Number ART960A;  7) 20GX3" RADIAL ART LINE KIT, Pack Number ART970A; 	 8) BIOPSY TRAY, Pack Number BT1015;  9) BIOPSY TRAY, Pack Number BT1060;  10) STEREOTACTIC BREAST BIOPSY TRAY, Pack Number BT1095;  11) BIOPSY KIT, Pack Number BT450A ;  12) CHEST TUBE INSERTION TRAY , Pack Number CHT1020;  13) CHEST TUBE INSERTION KIT, Pack Number CHT1465;  14) CHEST TUBE INSERTION TRAY , Pack Number CHT2040;  15) CHEST TUBE INSERTION TRAY , Pack Number CHT2040H ;  16) CHEST TUBE INSERTION TRAY, Pack Number CHT560;  17) CHEST TUBE INSERTION TRAY , Pack Number CHT701 ;  18) CHEST TUBE INSERTION TRAY, Pack Number CHT705;  19) CIRCUMCISION TRAY, Pack Number C

## 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-3020-2024
- **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-3020-2024

## Citation

> AI Analytics. FDA recall Z-3020-2024. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-3020-2024. Source: US FDA. Licensed CC0.

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