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FDA · Medical devices ·

STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530 recall

Stryker Corporation recalled STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530 on August 12, 2026 because of there has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. It was sold nationwide.

Why it was recalled

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

What's recalled

STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530

Quantity: 11,857 Units

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Stryker Corporation, San Jose, CA
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
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.
Status
Ongoing
Recall number
Z-2865-2026
Source
U.S. Food and Drug Administration

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