Preat Corp recalls multiple dental digital analog products due to out of specification rotation affecting dental abutment inspections. Affected models include NobelBiocare, Straumann, 3i Certain, and Astra-compatible items with specific model numbers and lot dates.
Due to a manufacturing issue, the product has a out of specification rotation of the digital analog used to visually inspect dental abutments and restorations.
Preat Corp is recalling several dental digital analog products that have an out of specification rotation. This issue could lead to inaccurate visual inspections of dental abutments and restorations during laboratory work.
The digital analogs have a rotation that is outside the specified tolerance. This can cause inaccurate visual inspections of dental abutments and restorations, potentially leading to incorrect dental work if not detected.
Dental laboratory professionals who use these digital analogs for inspecting dental abutments and restorations are most at risk. Affected products include specific models from NobelBiocare, Straumann, 3i Certain, and Astra brands.
Check for model numbers 9000703, 9001303, 9001903, 9002003, 9002103, 9002203, 9005203, 9005303, 9005403, 9005503, 9008503, or 9006767 on the product. Products sold with lot numbers 250219, 248890, 251432, 250602, 250418, 250213, 251459, 249071, 250335, 250223, 250336, 249510, or 250215 are also affected.
Identify the model number on the product to see if it matches the affected list: 9000703, 9001303, 9001903, 9002003, 9002103, 9002203, 9005203, 9005303, 9005403, 9005503, 9008503, or 9006767.
Check the lot number on the product to see if it is one of the affected lot numbers: 250219, 248890, 251432, 250602, 250418, 250213, 251459, 249071, 250335, 250223, 250336, 249510, or 250215.
Affected digital analogs include NobelBiocare Tri-Lobe-compatible 6.0mm, Straumann Tissue-Level-compatible WN, 3i Certain-compatible 5.0mm and 6.0mm, Astra-compatible 3.0mm, Aqua 3.5/4.0mm, Lilac 4.5/5.0mm, BioHorizons-compatible 3.0mm, Legacy-compatible 3.0mm, 3.5mm, and 5.7mm models with specific model numbers and lot dates.
Check the model number on the product. Affected models include 9000703, 9001303, 9001903, 9002003, 9002103, 9002203, 9005203, 9005303, 9005403, 9005503, 9008503, or 9006767. Also check the lot number against the affected list: 250219, 248890, 251432, 250602, 250418, 250213, 251459, 249071, 250335, 250223, 250336, 249510, or 250215.
The recall record does not specify a remedy, so no action is required beyond checking if your product is affected.
We’ve drafted a message you can send Preat Corp to request your refund or repair — edit it as you like.
Subject: Recall Z-2687-2024 — Preat Corp Preat Corp Hello, I own a Preat Corp that is covered by recall Z-2687-2024 from Preat Corp. 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.
