Stryker GmbH recalls Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;

Recall date

March 28, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1620-2025

FDA classification

Class II

Brand / firm

Stryker GmbH

Sold / distributed

US Nationwide distribution in the states of CA, GA, IL, KY, MA, MD, NY, OH, TN, TX, WV.

Why it was recalled

The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;