Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Osstem Implant System - Abutment ET Multi Abutment Size: 4.8D Recalled by Hiossen Inc. Due to Patient chart stickers provided inside the packaging may...
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 Hiossen Inc. directly.
Affected Products
Osstem Implant System - Abutment ET Multi Abutment Size: 4.8D 3.0G/H- Abutment is intended for use with a dental implant to provide suport for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETMTA503RV1
Quantity: 19 units
Why Was This Recalled?
Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hiossen Inc.
Hiossen Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report