Hiossen recalls specific dental abutment models due to incorrect chart stickers that may mislabel Mini versions as Regular and vice versa, potentially causing improper implant support.
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
Hiossen is recalling certain dental abutment models because their packaging stickers might incorrectly label Mini versions as Regular and vice versa. This could lead to improper implant support if the wrong type is used during dental procedures.
The packaging stickers may misidentify Mini abutments as Regular versions and Regular abutments as Mini versions. This could cause improper implant support if the wrong type is used during dental procedures, potentially affecting the stability of the dental restoration.
Dental professionals who use Hiossen ET Rigid Abutment (Mini) models with the specific model number ETRGA4537MP are likely affected. Patients receiving dental implants with these abutments may be at risk if the wrong version is used.
Check for the model number ETRGA453: 4.5D 3.0G/H 7.0H on the packaging. The lot code UDI-DI: 00814913026428 and lot number H4E20L088 are also associated with this specific recall.
Verify the model number on the packaging to ensure it matches ETRGA4537MP for the Mini version.
The recall is happening because the chart stickers inside the packaging may incorrectly label Mini abutments as Regular and vice versa, which could lead to improper implant support.
Check the model number on the packaging. If it matches ETRGA4537MP, you may need to verify the labeling with your dentist to ensure proper use.
The official recall does not provide a fix; users must check the labeling to ensure they are using the correct version for their dental implant procedure.
We’ve drafted a message you can send Hiossen to request your refund or repair — edit it as you like.
Subject: Recall Z-1272-2025 — Hiossen Hiossen Hello, I own a Hiossen that is covered by recall Z-1272-2025 from Hiossen. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
