Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Destino Twist 14F (also branded as Guidestar 14F) Recalled by Oscor Inc. Due to There is potential for separation between the threaded...
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 Oscor Inc. directly.
Affected Products
Destino Twist 14F (also branded as Guidestar 14F)
Quantity: 549 units
Why Was This Recalled?
There is potential for separation between the threaded hub and threaded cap at the proximal end of the device.
Where Was This Sold?
This product was distributed to 2 states: PA, TN
About Oscor Inc.
Oscor Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report