# FDA recall Z-3024-2024

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

## Product

Medline Convenience kits labeled as:    1) PREP TRAY, Pack Number DYNDA1540;   2) STERILE PREP TRAY , Pack Number DYNDA2499;   3) ED PREP TRAY, Pack Number DYNDA2519;   4) ED PREP TRAY, Pack Number DYNDA2519H ;   5) PRE-OP PREP KIT , Pack Number DYNDA3076;   6) PILGRIM PREP TRAY , Pack Number DYNDC3282;   7) PILGRIM PREP TRAY , Pack Number DYNDC3282A ;   8) PILGRIM PREP TRAY , Pack Number DYNDC3282B ;   9) KYPHO PREP PACK-LF, Pack Number DYNJ0618280G ;   10) KYPHO PREP PACK-LF, Pack Number DYNJ0618280I ;   11) KYPHO PREP PACK-LF, Pack Number DYNJ0618280J ;   12) SPECIAL PROCEDURE PREP TRAY-LF, Pack Number DYNJ0738967A ;   13) BASIC SET UP PACK-LF, Pack Number DYNJ28988I ;   14) BASIC SET UP PACK-LF , Pack Number DYNJ28988I ;   15) VERTEBRALPLASTY PREP TRAY PACK, Pack Number DYNJ36311A ;   16) PK-SETUP PACK , Pack Number DYNJ43804A ;   17) SKIN LESION PACK, Pack Number DYNJ44258G ;   18) SETUP PACK, Pack Number DYNJ46187D ;   19) PK-SET UP -LF , Pack Number DYNJ53220B ;   20) IR PATIENT

## 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.

## Key facts

- **Recall number:** Z-3024-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-08
- **Report date:** 2024-09-18

- **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-3024-2024

## Citation

> AI Analytics. FDA recall Z-3024-2024. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-3024-2024. Source: US FDA. Licensed CC0.

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