Medical device recalls Moderate risk

Hiossen Inc. recalls ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for use with a dental implant to provide support for prosthet…

Recall date
January 27, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1275-2025
FDA classification
Class II
Brand / firm
Hiossen Inc.
Sold / distributed
US Nationwide distribution.

Why it was 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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETRGA4524MP

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