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
FDA Recall Z-1274-2025 · Posted 2025-03-05
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Recalling FirmHiossen Inc.
Recall StatusOpen, Classified
Product CodeNHA
Date Initiated2025-01-27
Product Quantity19 units
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
Firm Action
Hoissen issued URGENT: MEDICAL DEVICE RECALL-CORRECTION letter on 1/27/25 via USPS Certified Mail. Letter states reason for recall, health risk and action to take.
Immediate Actions to be taken by You, the clinician:
1. Do not use the affected devices
2. Quarantine (separate) the affected devices in a different location, away from normal stock room.
3.Immediately fill out the Acknowledgement and Receipt Form* (Fax: 267-795-7031 or Email: [email protected] )
*Response is required regardless if the devices have already been return or implanted
4. Return quarantined devices to the following address or contact your sales representative for assistance.
ATTN: Peter Lee / Recall
85 Ben Fairless Dr.
Fairless Hills, PA 19030
5. Replacement patient chart stickers will be provided so that you may include the corrected chart sticker in the patient s medical records as applicable.
Hiossen has already deployed a permanent corrective action to address the issue described in this Recall Notice. Hiossen investigated and identified the source of the issue and has already implemented new procedures which eliminates the potential for further mis-labeling.
Other Information
If you need any further information or support concerning this recall/issue, please reach HIOSSEN:
Monday through Friday, 8:00 AM to 4:30 PM, Eastern Time.
Tel: 267-795-7031
Email: recall@hiossen
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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