# FDA recall Z-2752-2024

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

## Product

Medline procedural kits labeled as:    1) ARTHROGRAM TRAY, Pack Number MNS11965A;   2) ARTHROGRAPH TRAY, Pack Number MNS12670A;   3) CIRCUMCISION TRAY, Pack Number CIT6860A;   4) CIRCUMCISION TRAY, Pack Number CIT6715;   5) CIRCUMCISION TRAY, Pack Number DYNDA2271;   6) CIRCUMCISION TRAY, Pack Number CIT7020;   7) CIRCUMCISION TRAY, Pack Number CIT7210;   8) CIRCUMCISION TRAY, Pack Number CIT6720A;   9) CIRCUMCISION TRAY, Pack Number CIT6665;   10) CIRCUMCISION TRAY  , Pack Number CIT6050 ;   11) CIRCUMCISION TRAY W/OUT CLAMP, Pack Number CIT6925;   12) CIRCUMCISION TRAY WITHOUT CLAM, Pack Number CIT6255 ;   13) GLMI ARTHROGRAM KIT:PCL, Pack Number SPEC0300B;   14) MERCY MEDICAL CIRCUMCISION TRAY, Pack Number CIT6780;   15) NICU CIRCUMCISION TRAY W/OUT CLAMP, Pack Number CIT6920;   16) NICU PROCEDURE TRAY     , Pack Number UVT925 ;   17) NURSERY CIRCUMCISION TRAY, Pack Number CIT4845;   18) OSF SMMC CIRCUMCISION KIT, Pack Number CIT7095;   19) PERIPHERAL ULTRASOUND CATHETER INSERTION, 

## 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-2752-2024
- **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-2752-2024

## Citation

> AI Analytics. FDA recall Z-2752-2024. Retrieved 2026-09-24 from https://api.ai-analytics.org/recall/Z-2752-2024. Source: US FDA. Licensed CC0.

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