Paltop recalls Scan Abutment NP (Cat. No. 30-70102) 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 certain Scan Abutment NP dental impression devices made before July 21, 2021 because they may have orientation errors that delay dental restorations. This affects dentists and dental technicians using these devices for digital impressions.
The devices may have a 2-degree orientation error between the peak head and titanium base, and size engraving inconsistencies. These issues could cause delays in final dental restorations but do not pose immediate injury risks.
Dentists and dental technicians who use Paltop Scan Abutment NP devices for dental impressions made before July 21, 2021. Patients receiving dental work with these devices may be at slightly higher risk of delayed restorations.
Check for the product name 'Scan Abutment NP' with catalog number 30-70102. The devices were manufactured before July 21, 2021.
Verify the manufacturing date is before July 21, 2021 by checking the product label.
No, the recall does not require immediate stop use. The devices may have minor orientation errors that could delay restorations but do not pose immediate injury risks.
Check for the product name 'Scan Abutment NP' with catalog number 30-70102 and a manufacturing date before July 21, 2021.
Contact Paltop Advanced Dental Solutions directly for details on the remedy, as the recall record does not specify a remedy.
We’ve drafted a message you can send Paltop to request your refund or repair — edit it as you like.
Subject: Recall Z-0014-2022 — Paltop Paltop Hello, I own a Paltop that is covered by recall Z-0014-2022 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.
