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High risk Medical DevicesClass II

Medline Namic Guidewires Recall

Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0.035X260CM LT, Model Number: DYNJGWIRE20L; 2) GWIRE HYDRO 0.035 180CM ANG S, Model Number: DYNJ

Updated February 25, 2026

Medline has recalled certain Namic Guidewires used in medical procedures because their regulatory clearances have been rescinded and they should no longer be used clinically.

Is the Medline Industries, LP recalled? Yes. This product was recalled by FDA on February 25, 2026. Details below.

What is recalled

Medline Namic Guidewires in 30 models including: GUIDEWIRE 3MMJ 0.035X260CM LT (Model DYNJGWIRE20L), GWIRE HYDRO in multiple configurations with 0.035" or 0.038" diameter, ranging from 150cm to 260cm length in straight or angled styles (Models DYNJHWIRE100 through DYNJHWIRE130), and GDWIRE.035IN in 150cm and 180cm lengths with 3MMJ LT designation (Models DYNJGWIRE01L, DYNJGWIRE03L).

Am I affected

You're affected if your medical facility has any Medline Namic Guidewire with a model number starting with DYNJGWIRE or DYNJHWIRE in inventory or use.

What to do right now

Stop using these guidewires immediately. Contact Medline Industries, LP for instructions on return or replacement of affected units.

The hazard

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Brands affected

Medline Industries, LP
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-1829-2026
Classification
Class II
Recalled
February 25, 2026
Read the official notice

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