Class II
Medical Device Recall: Guide Wire with Ruler Tube 3x1000 mm DIA; Catalog number/REF: 2351-3100S;
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
6407 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1621-2025
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.