PlainRecalls
FDA Devices Moderate Class II Ongoing

ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETRGA4537MP

Reported: March 12, 2025 Initiated: January 27, 2025 #Z-1272-2025

Product Description

ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETRGA4537MP

Reason for Recall

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

Details

Recalling Firm
Hiossen Inc.
Units Affected
19
Distribution
US Nationwide distribution.
Location
Fairless Hills, PA

Frequently Asked Questions

What product was recalled?
ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETRGA4537MP. Recalled by Hiossen Inc.. Units affected: 19.
Why was this product 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
Which agency issued this recall?
This recall was issued by the FDA Devices on March 12, 2025. Severity: Moderate. Recall number: Z-1272-2025.