# FDA recall Z-2593-2026

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

## Product

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    ABDOMINAL VASCULAR-LF	  	DYNJ905291B  	DYNJ905291C  	  ARTERIOGRAM	  	DYNJ28082G  	  CVICU HEART BAG	  	DYKM2130A  	  ENDOVASCULAR PACK	  	DYNJ0678934J  	  EP PACK	  	DYNJ23456J  	  GENERAL ENDO PACK-LF	  	DYNJ0842873K  	  HYBRID PACK	  	DYNJ65925B  	DYNJ65925C  	  NON VASCULAR PACK	  	DYNJ68037  	  PACEMAKER	  	DYNJ901681D  	  PACEMAKER PACK	  	DYNJ51853C  	DYNJ51853D  	DYNJ60606A  	  PACER PACK	  	DYNJ40952A  	  RADIOLOGY VASCULAR ACCESS TRAY	  	DYNJVB1303A  	  SM- INTERVENTIONAL DRAPE PK-LF	  	DYNJ0780143K  	  VASCULAR ACCESS PACK-LF	  	DYNJ0101291D  	  VASCULAR DSC	  	DYNJ69172  	DYNJ69172B    VASCULAR HYBRID	  	DYNJ57543F  	DYNJ57543I  	DYNJ57543J  	  VASCULAR PACK	  	DYNJ61702A

## 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-2593-2026
- **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-2593-2026

## Citation

> MORVS. FDA recall Z-2593-2026. Retrieved 2026-10-17 from https://api.morvs.ai/recall/Z-2593-2026. Source: US FDA. Licensed CC0.

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