Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
HammerTube Implant Recalled by Paragon 28, Inc. Due to Due to Titanium plasma coating not present implant.
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 Paragon 28, Inc. directly.
Affected Products
HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)
Quantity: 9 implants
Why Was This Recalled?
Due to Titanium plasma coating not present implant.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Paragon 28, Inc.
Paragon 28, Inc. has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report