Class II

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

Stryker GmbH · March 28, 2025

Reason for Recall

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.

Distribution

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

States Affected

NATIONWIDE

Quantity Affected

1588 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1620-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Stryker GmbH Medical Device Recall: Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S; | SafeCheck