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Stryker Corporation recalls STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530
Recalled August 12, 2026 · FDA recall Z-2865-2026 · Stryker
Hazard
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. · FDA Class II
Units
11,857 Units
Sold at
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.
Description
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Product
STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530
Manufacturer(s)
Stryker Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →