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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