# FDA recall Z-1891-2026

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

## Product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes    ARTERIOGRAM TRAY	00-402001T, 00-402001U  	  CATH LAB-VEIN PROCEDURES	DYNJ60329A  	  CENTRAL VENOUS ACCESS PACK-LF	CVI5070  	  FISTULAGRAM PACK	DYNJ66259  	  INVASIVE LINE INSERTION	DYNJ44123C  	  NON VASCULAR PACK	DYNJ68037B, DYNJ68037C  	  PICC ABSCESS PACK-LF	DYNJ0774005G  	  PICC LINEPACK (PCLUI)642-LF	DYNJ47717B  	  PICC PHC	DYNJ37484C

## 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-1891-2026
- **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-1891-2026

## Citation

> AI Analytics. FDA recall Z-1891-2026. Retrieved 2026-07-04 from https://api.ai-analytics.org/recall/Z-1891-2026. Source: US FDA. Licensed CC0.

---

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