Paltop recalls Scan Abutment MU (Cat. No. 30-70103) made before July 21, 2021 due to potential 2-degree orientation errors that could delay dental restorations. Affected users should contact the manufacturer for details.
Some devices are outside tolerances and showed a maximal deviation of 2 degrees in the orientation between the peek head and titanium base, and an incongruence between the size engraved on the peek has been identified. Deviations may delay the final restoration.
Paltop recalls certain Scan Abutment MU dental implants made before July 21, 2021 because they may have orientation errors that could delay dental restorations. This affects dentists and dental technicians who use these implants for digital impressions.
The dental implants may have a 2-degree orientation error between the peak head and titanium base, and size discrepancies that could delay the final dental restoration process. These issues are not immediate safety hazards but affect the precision of dental work.
Dentists and dental technicians who use Paltop Scan Abutment MU implants for dental impressions. Patients receiving these implants are not directly affected by the recall.
Check for the product code 30-70103 and the manufacturing date before July 21, 2021. The product is used for taking dental impressions with intraoral scanners.
Verify the manufacturing date is before July 21, 2021 for affected units.
The Scan Abutment MU devices may have orientation errors that could delay dental restorations, but they do not pose an immediate safety risk.
No, the recall does not require immediate discontinuation. Affected users should check the product date and contact Paltop for further instructions.
Look for the product code 30-70103 and a manufacturing date before July 21, 2021.
We’ve drafted a message you can send Paltop to request your refund or repair — edit it as you like.
Subject: Recall Z-0015-2022 — Paltop Paltop Hello, I own a Paltop that is covered by recall Z-0015-2022 from Paltop. 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.
