# FDA recall Z-1102-2024

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

## Product

MEDLINE Kits, trays, and packs labeled as follows:    a)	ASC GENERAL MINOR CDS, REF CDS983673G;   b)	ASC GENERAL MINOR CDS, REF CDS983673I;   c)	C NURSE BAG KIT, REF DYKM1425;   d)	DAILY DRIVELINE MGMT KIT w/PER, REF DT18700;   e)	GASTRIC CULTURE PACK, REF DYNJ53966A;   f)	GASTRIC CULTURE PACK, REF DYNJ53966AH;   g)	HERNIA, REF CDS982034R;   h)	HERNIA, REF CDS982034S;   i)	HERNIA PACK, REF DYNJ39331B;   j)	LAP APPY PACK, REF DYNJ37709J;   k)	LAP CHOLE CDS, REF CDS983912V;   l)	LAP CHOLE CDS, REF CDS983912W;   m)	LAP CHOLE CDS, REF CDS983912X;   n)	LAP CHOLE CDS, REF CDS983912Y;   o)	LAPAROSCOPY PACK, REF DYNJ41417J;   p)	LAPAROTOMY CDS-LF, REF CDS860091A;   q)	LOWER EXTREMITY, REF DYNJ46222M;   r)	MAJOR PACK, REF DYNJ80578A;   s)	MINOR PACK, REF DYNJ67217D;   t)	N L MINOR CDS, REF CDS982518O;   u)	N L MINOR CDS, REF CDS982518P;   v)	NON STERILE I&D KIT, REF DYKM1438;   w)	PACK,GU MINOR, REF DYNJ906885B;   x)	PLASTICS SUTURE TRAY, REF SUT13535;   y)	RESPIRATORY KIT, REF DYKM1404;   z)	T

## 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-1102-2024
- **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-1102-2024

## Citation

> AI Analytics. FDA recall Z-1102-2024. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/Z-1102-2024. Source: US FDA. Licensed CC0.

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