# FDA recall Z-2594-2026

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

## Product

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    CENTRAL LINE TRAY	  	DYNJ41089  	  FISTULAGRAM PACK	  	DYNJ62827A  	  FISTULOGRAM PACK	  	DYNJ47899A  	  INVASIVE LINE INSERTION	  	DYNJ44123B  	  NON VASCULAR PACK	  	DYNJ68037A  	  VASCULAR ACCESS PACK-LF	  	DYNJ0101291F

## 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-2594-2026
- **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-2594-2026

## Citation

> MORVS. FDA recall Z-2594-2026. Retrieved 2026-10-18 from https://api.morvs.ai/recall/Z-2594-2026. Source: US FDA. Licensed CC0.

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