# FDA recall Z-3034-2024

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

## Product

Medline Convenience kits labeled as:    1) KIT, MIDSTREAM, W/BZK/FUNNL,3O, Pack Number DYND30212;   2) PROCESSING KIT 3 PTE0000204 , Pack Number DYNJ65728A ;   3) 30ML KIT, Pack Number DYNJ82155A ;   4) DISSECTION, Pack Number DYNJ85191;   5) FLAP HARVEST PACK , Pack Number DYNJ58575C ;   6) KIT, MIDSTREAM, W/BZK/FUNNL,3O, Pack Number DYND30212H ;   7) FLAP HARVEST PACK, Pack Number DYNJ58575C

## 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-3034-2024
- **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-3034-2024

## Citation

> AI Analytics. FDA recall Z-3034-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-3034-2024. Source: US FDA. Licensed CC0.

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