# FDA recall Z-2761-2024

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

## Product

Medline Procedure kits labeled as:    1) CIRCUMCISION SET, Pack Number CIT6335;   2) CIRCUMCISION TRAY , Pack Number CIT6135BH;   3) CIRCUMCISION TRAY , Pack Number CIT2465;   4) CIRCUMCISION TRAY , Pack Number CIT4920;   5) CIRCUMCISION TRAY , Pack Number CIT7455;   6) CIRCUMCISION TRAY , Pack Number DYNDA3045;   7) CIRCUMCISION TRAY , Pack Number DYNDL1889;   8) CIRCUMCISION TRAY , Pack Number CIT7455H ;   9) CIRCUMCISION TRAY W/1.3 CLAMP , Pack Number CIT6075;   10) CIRCUMCISON TRAY, Pack Number CIT7380;   11) HOSPITAL CIRCUMCISION T, Pack Number CIT2825;   12) CIRCUMCISION TRAY , Pack Number CIT6135A ;   13) CIRCUMCISION TRAY , Pack Number CIT6135B ;   14) NICU CIRCUMCISION SET, Pack Number CIT6900;

## 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-2761-2024
- **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-2761-2024

## Citation

> AI Analytics. FDA recall Z-2761-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2761-2024. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
