# FDA recall Z-1111-2024

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

## Product

Medline Kits, trays, and packs labeled as follows:    a)	709E RECOVERY PACK A,B,C II SS, REF DYNJ55960G;   b)	ABDOMEN PACK, REF DYNJ53643C;   c)	BAG TRUNK STOCK KIT, REF DYKM1880;   d)	BEDSIDE BRONCH PACK, REF DYKE1601;   e)	BIOPSY TRAY, REF DYNDH1242;   f)	BRONCH KIT, REF DYKE1840;   g)	BRONCHOSCOPY PACK, REF DYNJ37775F;   h)	BRONCHOSCOPY TRAY, REF DYNDL1350A;   i)	BRONCHOSCOPY TRAY, REF DYNDL1350AH;   j)	CAP CHANGE LARGE KIT, REF DYNDA2277A;   k)	CAP CHANGE LARGE KIT, REF DYNDA2277B;   l)	DAILY VAD DRIVELINE KIT, REF DYNDC3006;   m)	DAILY VENT KIT, REF DYNDJ1076;   n)	DIALYSIS OFF KIT, REF DT21230A;   o)	DIALYSIS OFF KIT, REF DT20350B;   p)	DIALYSIS ON KIT, REF DT20355B;   q)	DOUBLE HUB/CAP CHANGE KIT, REF DYNDC2843;   r)	DR D CUSTOM PACK, REF DYNJ68068A;   s)	DR D CUSTOM PACK, REF DYNJ68068B;   t)	DUODENUM CULTURING PACK, REF DYNJ51294;   u)	EGD SOUTHEASTERN REG KIT, REF DYKE1830;   v)	EMERGENCY UMBILICAL INSERTION, REF UVT1165;   w)	ENDO KIT, REF DYKE1069B;   x)	ENDO KIT, REF DYKE1

## 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-1111-2024
- **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-1111-2024

## Citation

> AI Analytics. FDA recall Z-1111-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1111-2024. Source: US FDA. Licensed CC0.

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