# FDA recall Z-1592-2025

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

## Product

Medline Convenience kits used for various procedures:  1) DR. KHAN CABG ADDS PACK, Model Number: DYNJ59310D;   2) CARDIAC STERNAL PACK, Model Number: DYNJ32436A;   3) VEIN CLOSURE PACK, Model Number: DYNJ35586G;   4) ABLATION PACK-LF, Model Number: DYNJ55343B;   5) ABLATION PACK-LF, Model Number: DYNJ55343B;   6) CARDIAC PACK, Model Number: DYNJ65027B;   7) VASCULAR PACK-LF, Model Number: DYNJ48196C;   8) IMPLANT PACK, Model Number: DYNJ40480;   9) OPEN HEART, Model Number: DYNJ900523B;   10) PACEMAKER PACK-LF, Model Number: DYNJ19758I;   11) CHOG VP SHUNT PACK, Model Number: SYNJ10280C;   12) VASCULAR PACK-LF, Model Number: DYNJ48196C;   13) EP PACK-LF, Model Number: DYNJ27949F;   14) PACEMAKER PACK WRO-LF, Model Number: DYNJ41874C;   15) CARDIAC PACK OPTION 1, Model Number: DYNJ83208A;   16) EP DRAPE PACK, Model Number: DYNJ56729;   17) CSTM EP PACEMAKER DRAPE PACK, Model Number: DYNJCD0326;   18) MINOR INTERVENTIONAL TRAY, Model Number: DYNJ80084;   19) CT PACK, Model Number: DYNJ39

## 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-1592-2025
- **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-1592-2025

## Citation

> AI Analytics. FDA recall Z-1592-2025. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1592-2025. Source: US FDA. Licensed CC0.

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