Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review of the packaging, it was...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Howmedica Osteonics Corp. directly.
Affected Products
Stryker, T2 Guidewire, Ball-Tipped, 3x800 mm Product Usage: Intended for the temporary stabilization of bone segments or fragments.
Quantity: 147,838 units in total
Why Was This Recalled?
During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Howmedica Osteonics Corp.
Stryker Howmedica Osteonics Corp. has 87 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report