# FDA recall Z-1881-2026

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

## Product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes      BARIATRIC	DYNJ905153M, DYNJ905153N  	  GENERAL LAPAROSCOPY PACK	DYNJ81602  	  LAPAROSCOPY	DYNJ905157K,	DYNJ905157L  	  LAPAROTOMY PACK	DYNJ46675G  	  MAJOR LITHOTOMY PACK	DYNJ81607  	  MAJOR PLUS PACK	DYNJ905160O    MINOR GENERAL PACK	DYNJ81599

## 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-1881-2026
- **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-1881-2026

## Citation

> AI Analytics. FDA recall Z-1881-2026. Retrieved 2026-08-13 from https://api.ai-analytics.org/recall/Z-1881-2026. Source: US FDA. Licensed CC0.

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