# FDA recall Z-1884-2026

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

## Product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes    ANGIO KIT PACK	DYNJ50783B  	  ANGIO PHC	DYNJ37485C	  	  C.I.C.N. ANGIO PACK	DYNJ53064B  	  FHT P NEURO PACK	DYNJ39931D	  	  NEURO ARTERIOGRAM PACK-LF	DYNJ0948060F	  	  NEURO KIT	NAM0003  	  NEURO PACK	DYNJ61542D  	  NEURO RADIOLOGY PACK	DYNJ59903B  	  NEURO TRAY	DYNJ84872A  	  PK, CATH LAB-ANGIO	DYNJ44027F  	  QVH IR NEURO PACK	DYNJ62176

## 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-1884-2026
- **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-1884-2026

## Citation

> AI Analytics. FDA recall Z-1884-2026. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1884-2026. Source: US FDA. Licensed CC0.

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