# FDA recall Z-1831-2026

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

## Product

Medline Syringes:  1) SYRINGE 12ML CONTROL W/ROTATOR, Model Number: DYNJSYR12CWR;   2) SYRINGE 10ML CONTROL W/ROTATOR, Model Number: DYNJSYR10CWR;   3) SYR CONTROL PAD 12ML L/L, Model Number: DYNJSYR12CP;   4) TBG PRESS 72IN M/F ROT BRAID, Model Number: DYNJBRT72R;   5) SYRINGE 10ML CONTROL MLL, Model Number: DYNJSYR10C;   6) SYRINGE 8ML CONTROL MLL, Model Number: DYNJSYR8C;   7) SYRINGE 12ML CONTROL MLL, Model Number: DYNJSYR12C;   8) SYR CONTROL PAD 10ML L/L ROT, Model Number: DYNJSYR10CRP;   9) SYR CONTROL PAD 12ML L/L ROT, Model Number: DYNJSYR12CRP;   10) CTRL SYRINGE 6ML RING ROT L/L, Model Number: DYNJSYRC6CWR

## 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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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-1831-2026
- **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-1831-2026

## Citation

> AI Analytics. FDA recall Z-1831-2026. Retrieved 2026-08-20 from https://api.ai-analytics.org/recall/Z-1831-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*