Lower riskMedical device recall · FDA · Published May 30, 2019
Paltop Advanced Plus Dental Implant Recall: Inconsistent Surface Topography Risk
Paltop recalls specific dental implants due to inconsistent surface topography. Affected units may have unreliable surface texture, potentially impacting dental procedures. Contact for details.
Surface micro/nano topography on some of the implants contained within this lot may not be consistently present over the entire surface of the implant.
Take action
Contact the company
📍Recalling firmPaltop Advanced Dental Solutions Ltd5, Ha-Shita · Caesarea, Israel
“Paltop Advanced Plus Dental Implant Recall: Inconsistent Surface Topography Risk.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/67818-paltop-advanced-plus-dental-implant-recall-inconsistent-surface-topography-risk. Based on FDA recall #Z-0019-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0019-2020%22&limit=1).
The FDA announced on May 30, 2019, that Paltop Advanced Dental Solutions Ltd voluntarily recalled Paltop Advanced Plus Dental Implants due to potential surface topography defects. The agency classified the recall as Class II.
How to tell if you have it
Brand: Paltop
Product: Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm
Catalog Number: 20-70024P
Lot Number: W0-008254
UDI: 729010869611020-70024P
The hazard
According to the FDA, the surface micro/nano topography on some of the implants contained within the recalled lot may not be consistently present over the entire surface of the implant.
Context
GovInfoNow's records show Paltop Advanced Dental Solutions Ltd has two other recalls on record since November 18, 2019. Other recent recalls of similar products include Straumann GM Helix Dental Implant Recall (July 13, 2026) and Straumann Dental Implant Abutments Recall (March 27, 2026).
How to tell if you have this one
Check for the model name 'Advanced Plus Dental Implant Dia 6.0mm L10mm', catalog number 20-70024P, and lot number W0-008254. The unique identifier (UDI) is 729010869611020-70024P.
Brand
Paltop
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Your Implant Details
Review the implant's model, catalog number, lot number, and unique identifier to confirm if it matches the recalled items.
Where it went and when
Where it was distributed
Distributed in 16 states.
Listed by the agency
Not listed
FDA distribution: “AL AZ CA CO FL GA MA MD MO MT NJ NM NY OH SC VA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arizona, California, Colorado, Florida, Georgia, Maryland, Massachusetts, Missouri, Montana, New Jersey, New Mexico, New York, Ohio, South Carolina, Virginia.
Recall timeline
FDA terminated this recall 12 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-0019-2020 (May 30, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0019-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.