# FDA recall Z-2590-2026

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

## Product

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    CATARACT FULL BODY	  	DYNJ85743  	  MAJOR VASCULAR PACK	  	DYNJ81610C  	  MINIMALLY INVASIVE PACK-LF	  	DYNJ0843063L  	  PEDIATRIC CATH ANGIO PACK	  	DYNJ54755J  	  PERIPHERAL ARTERIOGRAM RAD	  	DYNJ61383C  	  POSTERIOR SPINE PACK-LF	  	DYNJ0843339O  	  UPPER EXTREMITY	  	DYNJ61907A  	  VISCERAL ANGIOGRAM PACK-LF	          DYNJ0429121L

## Reason for recall

Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA.  Products not initially reported in RES 98601.

## Distribution

US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IL, KS,  KY, LA, MA, MD, MI, MN, MO, MS, MT, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, TN, TX, VA, WI,  WY and the country of Barbados.

## Key facts

- **Recall number:** Z-2590-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-02-27
- **Report date:** 2026-07-01

- **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-2590-2026

## Citation

> MORVS. FDA recall Z-2590-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2590-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*