# FDA recall Z-3042-2024

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

## Product

Medline Convenience kits labeled as:   1) ANGIOGRAPHY DRAPE PACK, Pack Number 00-401327AA;  2) CORONARY ANGIO PACK-LF, Pack Number 00-401594R ;  3) IR NEURO INTERVENTIONAL PACK, Pack Number 00-401808S ;  4) NEURO CDS , Pack Number CDS780056K ;  5) NEURO CDS , Pack Number CDS780056L ;  6) SHUNT CDS-LF, Pack Number CDS780103K ;  7) NEURO CDS , Pack Number CDS780108T ;  8) NEURO LAMINECTOMY-LF, Pack Number CDS780109M ;  9) NEURO LAMINECTOMY-LF, Pack Number CDS780109N ;  10) NEURO LAMINECTOMY-LF, Pack Number CDS780109O ;  11) NEURO CRANIOTOMY CDS #36-RF , Pack Number CDS780119T ;  12) NEURO CDS , Pack Number CDS780162AA;  13) NEURO CDS , Pack Number CDS780162AB;  14) NEURO CDS , Pack Number CDS780162AC;  15) NEURO CDS , Pack Number CDS780162AD;  16) NEURO CDS , Pack Number CDS780162X ;  17) NEURO CDS , Pack Number CDS780162Y ;  18) BASIC NEURO PROCEDURE , Pack Number CDS780202K ;  19) BASIC NEURO PACK, Pack Number CDS780202L ;  20) BASIC NEURO PACK, Pack Number CDS780202O ;  21) BASIC NEUR

## 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-3042-2024
- **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-3042-2024

## Citation

> AI Analytics. FDA recall Z-3042-2024. Retrieved 2026-08-24 from https://api.ai-analytics.org/recall/Z-3042-2024. Source: US FDA. Licensed CC0.

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