# FDA recall Z-1806-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-03-12.

## Product

namic CONVENIENCE KIT,   a) CAROTID MANIFOLD KIT, REF 60011045;   b) 3V MANIFOLD KIT ON WITH NAMIC DT & WASTE MANAGEMENT, REF 60070582;   c) LEFT HEART KIT, REF 60071822;   d) LEFT HEART KIT, REF 60080085;   e) CONVENIENCE KIT, REF 60100055;   f) CONVENIENCE KIT, REF 60101041;   g) CONVENIENCE KIT, REF 60120336;   h) LEFT HEART KIT, REF 60131446;   i) 3 VALVE MANIFOLD OFF KIT WITH SQUEEZE CONTRAST CONTROLLER AND PROTECTION  STATION, REF 60140798;   j) CONVENIENCE KIT, REF 60142592;   k) LEFT HEART KIT, REF 60183972;   l) FOUR VALVE MANIFOLD KIT, REF 60210209;   m) RIGHT HEART KIT, REF 60210862;   n) LEFT HEART KIT, REF 600705710;    o) CONVENIENCE KIT, REF 600803410;   p) TUBING KIT; REF 601322913;   q) LEFT HEART KIT, REF 60032582A

## Reason for recall

Products have a lack of sterility assurance.

## Distribution

US Nationwide distribution in the states of AL, FL, KY, MS, TX, WA, WI, NC, VA, CA, SD, TN, GA, PA, TX.

## Key facts

- **Recall number:** Z-1806-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-12
- **Report date:** 2024-05-22

- **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-1806-2024

## Citation

> AI Analytics. FDA recall Z-1806-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1806-2024. Source: US FDA. Licensed CC0.

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