# FDA recall Z-3059-2024

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

## Product

Medline Convenience kits, labeled as:     1) BLOOD CULTURE COLLECTION KIT, Pack Number BP115;   2) NICU CNTRL LINE BLOOD DRAW KIT, Pack Number DYLAB1044;   3) NEURO ANGIO PACK, Pack Number DYNDA1431A;   4) BLOOD WITHDRAWAL KIT #2, Pack Number DYNDA1683A;   5) LCPH LAB DRAW KIT , Pack Number DYNDH1641A ;   6) LCPH LAB DRAW KIT , Pack Number DYNDH1641AH;   7) INFUSION CENTER BLOOD DRAW KIT, Pack Number DYNDH1798;   8) BLOOD CULTURE, Pack Number DYNDH1921;   9) BLOOD WITHDRAWAL TRAY, Pack Number DYNDV1588F;   10) BLOOD WITHDRAWAL TRAY , Pack Number DYNDV1588G ;   11) PHLEBECTOMY PK, Pack Number DYNJ84749;   12) ARTHROGRAPH TRAY, Pack Number MNS12670A;   13) BLOOD CULTURE COLLECTION KIT, Pack Number MNS8915;   14) BLOOD CULTURE COLLECTION KIT, Pack Number MNS8915H ;   15) LACERATION TRAY, Pack Number SUT20955

## 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-3059-2024
- **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-3059-2024

## Citation

> AI Analytics. FDA recall Z-3059-2024. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-3059-2024. Source: US FDA. Licensed CC0.

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