Paltop Advanced Dental Solutions recalls Scan Abutment SP (Cat. No. 30-70101) made before July 21, 2021 due to possible 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 Scan Abutment SP 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 error between the peak head and titanium base, and size engraving discrepancies. These issues could cause delays in final dental restorations but do not cause injury.
Dental professionals using Scan Abutment SP devices for dental impressions made before July 21, 2021. Patients receiving dental implants are most at risk of delayed treatment.
Check for the product name 'Scan Abutment SP' with catalog number 30-70101. Devices manufactured before July 21, 2021 are affected.
Reach out to Paltop Advanced Dental Solutions for specific details about your device and next steps.
No, the recall does not mention injury risk. The issue may delay dental restorations.
The devices may have a 2-degree orientation error between the peak head and titanium base, and size engraving discrepancies 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-0013-2022 — Paltop Paltop Hello, I own a Paltop that is covered by recall Z-0013-2022 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.
