# FDA recall Z-1112-2024

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

## Product

Medline Kits, trays, and packs labeled as follows:    a) LACERATION KIT, REF SUT13935;   b) LACERATION TRAY, REF SUT21215;   c) LACERATION TRAY, REF SUT15380;   d) LACERATION TRAY W/SNAGFREE NEE, REF SUT19005;   e) PLASTICS SUTURE TRAY, REF SUT13535;   f) UVC INSERTION TRAY, REF UVT840A  g) BRONCHOALVEOLAR LAVAGE PACK, REF DYNDA2369A;   h) CENTRAL LINE NEEDLELESS CONNECTOR KIT, REF DYNDC2869B;   i) CVC STERILE CAP CHANGE KIT, REF DT20900A;   j) DOUBLE VALVE CHANGE KIT, REF DYNDA2660A;   k) KIDNEY BIOPSY PACK, REF DYNDH1650;   l) PORT ACCESS INFUSION KIT - 0.75IN NEEDLE, REF DYNDC2816C;   m) PORT ACCESS KIT, REF EBSI1302A;   n) SHORT TERM INFUSAPORT ACCESS KIT, REF DYNDC3188;   o) SINGLE VALVE CHANGE KIT, REF DYNDA2659A;   p) SUTURE TRAY, REF DYNDS1085A;

## 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-1112-2024
- **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-1112-2024

## Citation

> AI Analytics. FDA recall Z-1112-2024. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-1112-2024. Source: US FDA. Licensed CC0.

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