# FDA recall Z-1833-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-02-25.

## Product

Medline Kits:  1) SYR CNTRL 10ML RING W/ROT NB, Model Number: DYNJSYR10CWRB;   2) MANIFOLD KIT LOW PRESSURE OFF, Model Number: VASCSLPOFF1;   3) EP MANIFOLD KIT, Model Number: VASC1018A

## Reason for recall

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1833-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-02-25
- **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-1833-2026

## Citation

> AI Analytics. FDA recall Z-1833-2026. Retrieved 2026-07-12 from https://api.ai-analytics.org/recall/Z-1833-2026. Source: US FDA. Licensed CC0.

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