Hiossen recalls specific dental abutment models due to incorrect chart stickers that may mislabel Mini versions as Regular and vice versa, risking 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 the chart stickers inside the packaging incorrectly identify Mini versions as Regular and vice versa. This could lead to improper implant support if the wrong size is used during dental procedures.
The chart stickers inside the packaging may mislabel Mini abutments as Regular and Regular abutments as Mini. This could cause improper implant support if the wrong size is used during dental procedures, potentially affecting the stability of the dental restoration.
Dental professionals using Hiossen ET Rigid Abutment (Mini) models with the specific model numbers and lot codes listed in the recall. Patients receiving dental implants using these abutments may be at risk if the wrong size is applied.
Check for the model numbers ETRGA4544MP and lot codes starting with H4E20L090. The product is intended for dental implants to support crowns, bridges, or overdentures.
Look for the model number ETRGA4544MP and lot code starting with H4E20L090 on the packaging.
The chart stickers inside the packaging may incorrectly identify Mini versions as Regular and vice versa, which could lead to improper implant support.
Check the product labels for model number ETRGA4544MP and lot code starting with H4E20L090. If you have the correct model, no action is needed.
The recall addresses potential mislabeling that could affect implant support, but the hazard does not indicate a risk of serious injury in normal use.
We’ve drafted a message you can send Hiossen to request your refund or repair — edit it as you like.
Subject: Recall Z-1273-2025 — Hiossen Hiossen Hello, I own a Hiossen that is covered by recall Z-1273-2025 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.
