Class II

Medical Device Recall: STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530

Stryker Corporation · June 8, 2026

Reason for Recall

There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.

Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Chile, France, Germany, Indonesia, Italy, Mexico, Netherlands, New Zealand, Philippines, South Korea, Spain, Sweden, Switzerland, Taiwan, United Kingdom.

States Affected

NATIONWIDE

Quantity Affected

11,857 Units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2865-2026

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.