# FDA recall Z-1890-2026

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

## Product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes    ADD A ENDOVASCULAR PACK-LF	DYNJ0429339L, DYNJ0429339M  	  ANGIO ARTERIOGRAM PACK-LF	DYNJ0774026K  	  ANGIO KIT PACK	DYNJ83746B  	  ANGIO TRAY NO LIDO	DYNJ85557A  	  ANGIOGRAPHY PACK II	DYNJ17218S, DYNJ17218T    ARTERIOGRAM NEURO PACK-LF	DYNJ0842499L  	  ARTERIOGRAM PACK-LF	DYNJ0842478M  	  CARDIAC CATH II PK	DYNJ21259O  	  CARDIAC CATH PACK	DYNJ68653D  	  CATH LAB ANGIOGRAPHY PACK	DYNJ50779G  	  CATH LAB-LF	DYNJ51423G  	  CRANIOTOMY PACK-LF	DYNJ0101292I  	  DEEP BRAIN STIMULATION PACK	DYNJ0842793I  	  ENDO VASCULAR MINOR	DYNJ87263  	  GENERAL ENDO PACK-LF	DYNJ0842873L  	  LEFT HEART	DYNJ45984J  	  LIPO PACK	DYNJ87218  	  MAA Y90 TRAY	DYNJ82191D  	  MAIN OR CATH LAB	DYNJ61373B  	  MINIMALLY INVASIVE PACK-LF	DYNJ0843063M  	  NEURO CERVICAL PACK	DYNJ0101287M  	  NEURO RADIOLOGY RICHMOND	DYNJ68365F  	  NEURO VP SHUNT PACK-LF	DYNJ0843121L  	  NON-VASCULAR PACK	DYNJ56386C, DYNJ56386D  	  OR ANGIOGRAM PA

## 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-1890-2026
- **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-1890-2026

## Citation

> AI Analytics. FDA recall Z-1890-2026. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1890-2026. Source: US FDA. Licensed CC0.

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