# FDA recall Z-1132-2024

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

## Product

Centurion Kits, trays, and packs labeled as follows:    a) BASIC PROCEDURE TRAY, REF MNS13600;   b) BWH DAILY DRIVELINE MGMT KIT, REF DM640A;   c) CIRCUMCISION TRAY, REF CIT6180;   d) INCISION & DRAINAGE TRAY, REF ID1690;   e) LACERATION TRAY, REF SUT19510;   f) LACERATION TRAY, REF SUT19510;   g) LACERATION TRAY, REF SUT8565;   h) LACERATION TRAY, REF SUT8565;   i) LINE REPAIR KIT, REF MNS12045A;   j) MMC DAILY DRIVELINE MGMT KIT, REF DM850A;   k) NEWBORN THORACOTOMY TRAY, REF MNS3470;   l) NICU STERILE CENTRAL LINE CHANGE KIT, REF DT18520A;   m) OMMAYA KITS - LATEX FREE, REF HT2375;   n) PEDIATRIC ULTRASOUND KIT, REF MNS12995A;   o) PORT ACCESS INFUSION KIT - 1IN NEEDLE, REF DYNDC2817C;   p) WOUND CLOSURE AND IRRIGATION TRAY, REF SUT14785;

## 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-1132-2024
- **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-1132-2024

## Citation

> AI Analytics. FDA recall Z-1132-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1132-2024. Source: US FDA. Licensed CC0.

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