# FDA recall Z-2444-2024

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

## Product

Medline procedure kits labeled as:    1) WMC HYBRID OR PACK PART 1 , Pack Number CMPJ08068F ;   2) VASCULAR PACK , Pack Number CMPJ11455B ;   3) SALEM CATH LAB-LF , Pack Number DYNJ26938J ;   4) EH PEDIATRIC CATH , Pack Number DYNJ49920L ;   5) ARTERIOGRAM PACK, Pack Number DYNJ53018;   6) CATH PACK , Pack Number DYNJ57729C ;   7) PEDS CATH PACK, Pack Number DYNJ66856;   8) PEDS CATH PACK, Pack Number DYNJ66856A ;   9) STEWARD ROCKLEDGE CATH RRS, Pack Number DYNJ81061A ;   10) CATH LAB PACK , Pack Number DYNJ84617;   11) UA/UV CATHETERIZATION TRAY, Pack Number UVT1190A

## 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: US (nationwide) and OUS countries of: AE, AI, BB, CA, CL, CY, DE, GT, HN, JP, MX, MY, PA, PE, PR, SA, SG, TC, TT, VI, PR, TT, MX, BM, ES, NI, DO, GU, CR, AT, CD, DE, DF, W, and ON.

## Key facts

- **Recall number:** Z-2444-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-08
- **Report date:** 2024-08-14

- **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-2444-2024

## Citation

> AI Analytics. FDA recall Z-2444-2024. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-2444-2024. Source: US FDA. Licensed CC0.

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