Paltop Advanced Dental Solutions recalls Scan Abutment PCA (Cat. No. 30-70105) made before July 21, 2021 due to potential 2-degree orientation deviations that may 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 PCA 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.
Dentists and dental technicians who use Paltop Scan Abutment PCA devices made before July 21, 2021. Patients receiving dental implants may be affected if their restorations are delayed.
Check for the product name 'Scan Abutment PCA' with catalog number 30-70105. The devices were made before July 21, 2021.
Verify the manufacturing date is before July 21, 2021.
The devices may have orientation deviations that could delay dental restorations, but they do not cause injury.
No, but you should check if your device was made before July 21, 2021 to see if it needs verification.
Look for the catalog number 30-70105 and check if it was manufactured 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-0017-2022 — Paltop Paltop Hello, I own a Paltop that is covered by recall Z-0017-2022 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.
