Clinician's Choice recalls Affinity Hydroactive Impression Material Heavy Body Regular Set 12PK due to incorrect compression material packaging. This could lead to improper dental impressions if used.
Wrong compression material - Template Ultra Quick matrix Material was packaged instead of the Heavy Body viscosity as indicated on the outer packaging of the 12PK
Clinician's Choice is recalling Affinity Hydroactive Impression Material Heavy Body Regular Set 12PK because the product contains the wrong compression material (Ultra Quick matrix) instead of the Heavy Body viscosity as labeled. Using this incorrect material could result in improper dental impressions.
The product contains Ultra Quick matrix material instead of the Heavy Body viscosity as labeled. This incorrect material could lead to improper dental impressions if used, potentially affecting the accuracy of the dental model.
Dental professionals who own or use the Affinity Hydroactive Impression Material Heavy Body Regular Set 12PK (product ID: 013912, lot number 611612) are affected. Dental technicians and dentists using this specific set are most at risk.
Check for product ID 013912 and lot number 611612 on the packaging. The product is a vinyl poly siloxane impression material sold by Clinician's Choice Dental Products Inc.
Verify the product ID (013912) and lot number (611612) on the packaging to confirm if it is recalled.
The product contains the wrong compression material, so it is not safe for use as intended. Using it could lead to improper dental impressions.
The recall does not specify a remedy, so check the product details to confirm if it is recalled and contact Clinician's Choice for further instructions.
Look for product ID 013912 and lot number 611612 on the packaging. The product is a vinyl poly siloxane impression material sold by Clinician's Choice Dental Products Inc.
We’ve drafted a message you can send Clinician's Choice to request your refund or repair — edit it as you like.
Subject: Recall Z-1100-2022 — Clinician's Choice Clinician's Choice Hello, I own a Clinician's Choice that is covered by recall Z-1100-2022 from Clinician's Choice. 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.
