# FDA recall Z-2751-2024

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

## Product

Medline procedural kits labeled as:    1) DRAWER 3 LAB DRAW & IV START, Pack Number ACC010417 ;   2) DRAWER 3 LAB DRAW & IV START, Pack Number ACC010417A;   3) DRAWER 9L , Pack Number ACC010427A;   4) MEDICATION DELIVERY MODULE, Pack Number ACC010605 ;   5) DRAWER 3, Pack Number ACC010641 ;   6) NEONATAL DRAWER 6 , Pack Number ACC010653 ;   7) DRAWER 2, Pack Number ACC010690 ;   8) ****, Pack Number ACC010690 ;   9) DRAWER 3, Pack Number ACC010784 ;   10) NURSERY CIRCUMCISION TRAY, Pack Number CIT4845;   11) CIRCUMCISION KIT, Pack Number CIT6535;   12) CIRCUMCISION TRAY, Pack Number CIT6720;   13) CIRCUMCISION TRAY, Pack Number CIT6720A;   14) MEDICAL CIRCUMCISION TRAY, Pack Number CIT6780;   15) NICU CIRCUMCISION TRAY W/OUT CLAMP, Pack Number CIT6920;   16) CIRCUMCISION TRAY W/OUT CLAMP, Pack Number CIT6925;   17) OSF SMMC CIRCUMCISION KIT, Pack Number CIT7095;   18) RETINA LAC/USC PACK , Pack Number CMPJ03205D;   19) AAA PACK-LF, Pack Number CMPJ09869B;   20) ****, Pack Number CMPJ21

## 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-2751-2024
- **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-2751-2024

## Citation

> AI Analytics. FDA recall Z-2751-2024. Retrieved 2026-08-03 from https://api.ai-analytics.org/recall/Z-2751-2024. Source: US FDA. Licensed CC0.

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