Paltop Advanced Dental Solutions recalls Scan Abutment SU (Cat. No. 30-70104) made before July 21, 2021 due to possible 2-degree orientation deviations 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 Scan Abutment SU dental impression devices made before July 21, 2021 because they may have orientation errors that delay dental restorations. This issue does not cause injury but could affect treatment timing.
The devices may have a 2-degree orientation deviation between the peak head and titanium base, and size engraving inconsistencies. These issues could cause delays in final dental restorations but do not cause injury.
Dental professionals using Scan Abutment SU devices made before July 21, 2021. Patients receiving dental implants are most at risk of delayed restorations.
Check for the product name 'Scan Abutment SU' and catalog number 30-70104. Devices manufactured before July 21, 2021 are affected.
Reach out to Paltop Advanced Dental Solutions for specific guidance on affected units and next steps.
No, the recall does not require immediate discontinuation. Affected users should contact the manufacturer for details.
The devices may have a 2-degree orientation deviation between the peak head and titanium base, and size engraving inconsistencies that could delay dental restorations.
Devices manufactured before July 21, 2021 are affected.
We’ve drafted a message you can send Paltop to request your refund or repair — edit it as you like.
Subject: Recall Z-0016-2022 — Paltop Paltop Hello, I own a Paltop that is covered by recall Z-0016-2022 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.
