# FDA recall Z-1887-2026

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

## Product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes    EXTREMITY PACK	DYNJ34846C  	  HAND PACK	DYNJ83218A, DYNJ85396  	  LAMINECTOMY	DYNJ905156R  	  MAJOR EXTREMITY	DYNJ905159L, DYNJ905159M  	  MAJOR EXTREMITY PACK	DYNJ69926A  	  PODIATRY PACK	DYNJ41250B

## 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-1887-2026
- **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-1887-2026

## Citation

> AI Analytics. FDA recall Z-1887-2026. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-1887-2026. Source: US FDA. Licensed CC0.

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