# FDA recall Z-2768-2024

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

## Product

Centurion procedure kits labeled as:   1) 3" RADIAL ARTERIAL LINE KIT- ICU, Pack Number ART240B;  2) 5FR 2L PICC LINE TRAY, Pack Number PICC0020;  3) 6" FEMORAL ARTERIAL  LINE KIT, Pack Number ART245B;  4) ADVANCED REPAIR KIT, Pack Number SUT15940;  5) ARTHROGRAM TRAY, Pack Number SPEC0004C;  6) ARTHROGRAM TRAY, Pack Number DYNDH1134;  7) ARTHROGRAM TRAY-LF, Pack Number SPEC0400;  8) ARTHROGRAM/LP/MYELOGRAM TRAY, Pack Number PT220;  9) AULTMAN HOSPITAL CHEST TUBE INSERTION TR, Pack Number CHT500;  10) BIOPSY BASIC PACK, Pack Number P784604;  11) BIOPSY KIT, Pack Number DYNDA1466A;  12) BIOPSY SKIN/LACERATION TRAY, Pack Number SUT20455;  13) BIOPSY TRAY, Pack Number BT1015;  14) BIOPSY TRAY, Pack Number DYNDH1273;  15) BIOPSY TRAY, Pack Number BT1060;  16) BIOPSY TRAY, Pack Number DYNDH1340;  17) BIOPSY TRAY, Pack Number P151659;  18) BIOPSY TRAY, Pack Number SPEC0292;  19) BIOPSY TRAY, Pack Number DYNDH1314A;  20) BIOPSY TRAY, Pack Number DYNDH1137C;  21) BIOPSY TRAY - LF, Pack Number 

## 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

## Key facts

- **Recall number:** Z-2768-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-08
- **Report date:** 2024-09-04

- **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-2768-2024

## Citation

> AI Analytics. FDA recall Z-2768-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2768-2024. Source: US FDA. Licensed CC0.

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