# FDA recall Z-1136-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class I · device recall initiated 2023-11-15.

## Product

Centurion Kits, trays, and packs labeled as follows:    a) A C DAILY WET KIT, REF DM405A;   b) BWH DAILY DRIVELINE MGMT KIT, REF DM640;   c) DAILY DRIVELINE MGMT SYSTEM, REF DM600;   d) DAILY MAINTENANCE SYSTEM LVAD, REF DM870A;   e) DAILY MAINTENANCE SYSTEM LVAD, REF DM870A;   f) DRESSING CHANGE TRAY WITHOUT DRESSING, REF DT21465B;   g) DRIVELINE MANAGEMENT SYSTEM, REF DT18905;   h) DRIVELINE MANAGEMENT SYSTEM-DAILY, REF DM610;   i) DRIVELINE MGMT TRAY W/O ANCHOR, REF DT18210;   j) DRIVELINE MGMT. KIT WITH SILVER ALGINATE, REF DT18695A;   k) LVAD DAILY PATIENT CHANGE KIT, REF DM630;   l) LVAD DAILY PATIENT CHANGE KIT, REF DM630;   m) LVAD DRIVELINE MGMT KIT, SENSITIVE SKIN, REF DT19005A;   n) LVAD MAINTENANCE KIT - LESS THAN 6 MOS., REF DM1060;   o) LVAD SENSITIVE KIT, REF DM525A;   p) MMC DAILY DRIVELINE MGMT KIT, REF DM850;   q) PATIENT DRESSING CHANGE  KIT SW, REF DT17355;   r) PEDIATRIC PORT ACCESS BUNDLE, REF DT19835B;   s) PORT ACCESS KIT, REF DT22575A;   t) PORT ACCESS TRAY, RE

## Reason for recall

Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components):  0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.

## Distribution

Distribution US nationwide including Puerto Rico, Canada, UAE, and Panama

## Key facts

- **Recall number:** Z-1136-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-15
- **Report date:** 2024-03-06

- **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-1136-2024

## Citation

> AI Analytics. FDA recall Z-1136-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1136-2024. Source: US FDA. Licensed CC0.

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