Hiossen recalls ET Rigid Abutment (Mini) models due to incorrect chart stickers that may mislabel Mini as Regular or Multi as Mini versions, risking wrong 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 recalls specific dental implant abutment models because packaging stickers incorrectly identify Mini versions as Regular or Multi versions. Using the wrong type could lead to improper implant support.
Incorrect chart stickers may label Mini abutments as Regular or Multi abutments as Mini. This could cause dental professionals to use the wrong abutment type, potentially leading to improper implant support.
Dental professionals using Hiossen ET Rigid Abutment (Mini) models for dental implants. Patients receiving these implants are at risk if the wrong abutment type is used.
Check for model number ETRGA4524MP and lot code H4E21G062 on the packaging. The product is sold for dental implants to support crowns, bridges, or overdentures.
Verify the model number and lot code on the packaging to confirm it matches ETRGA4524MP and H4E21G062.
The recall is due to incorrect chart stickers that may mislabel Mini abutments as Regular or Multi abutments as Mini, which could lead to improper implant support.
Check the product label for model number ETRGA4524MP and lot code H4E21G062. If it matches, you may continue using it but verify the correct type.
The recall addresses potential mislabeling that could lead to improper implant support, but no specific injury risk is stated.
We’ve drafted a message you can send Hiossen to request your refund or repair — edit it as you like.
Subject: Recall Z-1275-2025 — Hiossen Hiossen Hello, I own a Hiossen that is covered by recall Z-1275-2025 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.
