Is Stryker Corporation recalled?

Yes — a recall has been published. Reason: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.

TemporaryFDAOngoing

Can cause harm that is usually temporary.

STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640

Check the device or its packaging for

GTIN 07613327061475, Batch Number: 24284FG2, 24289FG2, 24313FG2, 24322FG2, 24338FG2, 24344FG2, 24351FG2, 25009FG2, 25036FG2, 25062FG2, 25091FG2, 25129FG2, 25161FG2.

Why: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Distributed: 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.
Company: Stryker Corporation
Announced: 12 August 2026This is the date the recall was announced. A company may have started it weeks earlier.
Recall began: 8 June 2026

Source: FDA record Z-2864-2026 · retrieved 3 August 2026

Read the official notice

Every recall is shown word for word from the FDA and USDA, with a link to the source.