# FDA recall Z-1593-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2025-03-03.

## Product

Medline Convenience kits used for various procedures:  1) LINE INSERTION PACK, Model Number: DYNJ44949C;   2) PICC LINE INSERTION BJC-LF, Model Number: DYNJ41682C;   3) SUPERFICIAL VENOUS PROCEDURE, Model Number: DYNJ81267A;   4) ILR INSERTION-REMOVAL PACK, Model Number: DYNJ82437A;   5) C LINE INSERTION CDS, Model Number: CDS980379J;   6) BSHR PICC LINE-LF, Model Number: DYNJ24529M;   7) ENSEMBLE POWER PICC-HEJ-LF, Model Number: DYNJ65827;   8) PICC LINE PACK, Model Number: DYNJ55170F;   9) LINE INSERTION PACK, Model Number: DYNJ44949C;   10) RFA PACK, Model Number: DYNJ67899A;   11) KIT CENTRAL LINE INSERTION-LF, Model Number: PHS902533005;   12) INFANT LUMBAR PUNCTURE TRAY, Model Number: DYNDH1904;   13) PICC PACK-LF, Model Number: DYNJ55356A;   14) GENERAL TRAY, Model Number: DYNJ15652M;   15) CVR ENDOVENOUS PACK, Model Number: DYNJ80643;   16) LINE INSERTION TRAY, Model Number: DYNJ20803D

## Reason for recall

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

## Key facts

- **Recall number:** Z-1593-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-03
- **Report date:** 2025-04-23

- **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-1593-2025

## Citation

> AI Analytics. FDA recall Z-1593-2025. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1593-2025. Source: US FDA. Licensed CC0.

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