Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Formula Shaver Handpiece (with buttons) Recalled by Stryker Endoscopy Due to Stryker Endoscopy determined that there may not have...
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 Endoscopy directly.
Affected Products
Formula Shaver Handpiece (with buttons); Formula 180 Shaver Handpiece (with button) Rx only, Made USA.: Stryker Endoscopy 5900 Optical Court San Jose, CA 95138 Components within the Crossfire System that provided abrasion, resection, debridement and removal of bone and soft tissue through the Formula Shaver and blade, and the ablation and coagulation of soft tissue, as well as hemostasis of blood vessels through its SERFAS Energy electrosurgical probe.
Quantity: 34 devices
Why Was This Recalled?
Stryker Endoscopy determined that there may not have been adequate determination of required routine checks to ensure accuracy and fitness for use of specific serial numbers of Formula and 180 Shaver Hand Control.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Endoscopy
Stryker Endoscopy has 238 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report