# FDA recall Z-1829-2026

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

## Product

Medline Namic Guidewires:  1) GUIDEWIRE 3MMJ 0.035X260CM LT, Model Number: DYNJGWIRE20L;   2) GWIRE HYDRO 0.035 180CM ANG S, Model Number: DYNJHWIRE105;   3) GWIRE HYDRO 0.035 260CM ANG S, Model Number: DYNJHWIRE107;   4) GWIRE HYDRO 0.035 260CM STR S, Model Number: DYNJHWIRE115;   5) GWIRE HYDRO 0.035 150CM STR, Model Number: DYNJHWIRE108;   6) GWIRE HYDRO 0.035 150CM ANG S, Model Number: DYNJHWIRE104;   7) GWIRE HYDRO 0.035 180CM STR S, Model Number: DYNJHWIRE113;   8) GWIRE HYDRO 0.035 260CM ANGLE, Model Number: DYNJHWIRE103;   9) GDWIRE .035INX150CM 3MMJ LT, Model Number: DYNJGWIRE01L;   10) GDWIRE .035INX180CM 3MMJ LT, Model Number: DYNJGWIRE03L;   11) GWIRE HYDRO 0.035 150CM STR S, Model Number: DYNJHWIRE112;   12) GWIRE HYDRO 0.035 180CM STR, Model Number: DYNJHWIRE109;   13) GWIRE HYDRO 0.035 210CM ANGLE, Model Number: DYNJHWIRE102;   14) GWIRE HYDRO 0.035 210CM ANG S, Model Number: DYNJHWIRE106;   15) GWIRE HYDRO 0.035 210CM STR, Model Number: DYNJHWIRE110;   16) GWIRE,HYDRO,0

## 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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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-1829-2026
- **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-1829-2026

## Citation

> AI Analytics. FDA recall Z-1829-2026. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1829-2026. Source: US FDA. Licensed CC0.

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