FDA recall record

Paltop Advanced Dental Solutions Scan Abutment NP, Cat recall — FDA Z-0014-2022

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…

Class IIclassification
Z-0014-2022official record ID
Oct 13, 2021report date

Recall record at a glance

Official recordZ-0014-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPaltop Advanced Dental Solutions Ltd
Report dateOct 13, 2021
Recall initiation dateJul 26, 2021
Quantity354
LocationCaesarea, Israel

Official product description

Scan Abutment NP, Cat. No. 30-70102 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient s chewing function.

Why the product was recalled

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.

Distribution information

US Nationwide distribution. No foreign distribution from US.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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