# FDA recall Z-1876-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-02-27.

## Product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes      JUDKINS PACK DYNJ51126    ANGIO PACK	DYNJ32555C, DYNJ66631  	  ANGIO TRAY	DYNJ46153B  	  ANGIOGRAPHY PACK	DYNJ26855F  	  ANGIOGRAPHY PACK-M-LF	DYNJ24530I  	  ANGIOGRAPHY TRAY-LF	DYNJ0220880V, DYNJ30077D  	  CATH LAB ANGIO PACK-LF	DYNJ0545064X  	  CATH LAB PACK	DYNJ39057C  	  FEMORAL ANGIOGRAPY SET UP	DYNJ61015B  	  RAD-ANGIO PACK	DYNJ47710C  	  SURGERY ANGIO PACK-LF	PHS677784013A

## Reason for recall

Unapproved design changes to the products outside of the 510(k) clearance.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados.

## Key facts

- **Recall number:** Z-1876-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-02-27
- **Report date:** 2026-04-29

- **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-1876-2026

## Citation

> AI Analytics. FDA recall Z-1876-2026. Retrieved 2026-07-03 from https://api.ai-analytics.org/recall/Z-1876-2026. Source: US FDA. Licensed CC0.

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