Paltop recalls specific dental implants due to incorrect screw packaging. The Standard Platform Cover Screw won't fit the Narrow Platform implant, causing potential misfit issues.
Some of the implants were packaged with a Standard Platform Cover Screw instead of a Narrow Platform Cover Screw. The Standard Platform Cover Screw will not fit in the Narrow Platform implant.
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Contact the company
📍Recalling firmPaltop Advanced Dental Solutions Ltd5, Ha-Shita · Caesarea, Israel
“Palt: Dynamic Dental Implant Recall - Wrong Screw Package Hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/66511-palt-dynamic-dental-implant-recall-wrong-screw-package-hazard. Based on FDA recall #Z-0836-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0836-2020%22&limit=1).
Paltop Advanced Dental Solutions Ltd voluntarily recalled Paltop Dynamic Dental Implants on Nov. 18, 2019, according to the FDA. The company said some units were packaged with incorrect cover screws that will not fit the implants.
How to tell if you have it
Brand: Paltop
Product: Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm
Catalog Number: 21-70020
Lot Number: WO-011320
The hazard
The FDA said some implants were packaged with a Standard Platform Cover Screw instead of a Narrow Platform Cover Screw. The record states the Standard Platform Cover Screw will not fit in the Narrow Platform implant.
Context
GovInfoNow's records show Paltop Advanced Dental Solutions Ltd has two other recalls on record since May 30, 2019. Other recent recalls of similar products include Paltop Scan Abutment MU: 2-Degree Orientation Deviation May Delay Dental Restorations (July 26, 2021) and Paltop Advanced Plus Dental Implant Recall: Inconsistent Surface Topography Risk (May 30, 2019). Other recent recalls of similar products include Straumann Dental Implant Abutments Recall: Incorrect Screw Seat Interface Hazard (March 27, 2026), Straumann Dental Implant Abutments Recall: Incorrect Screw Seat Interface (March 27, 2026), and Straumann GM Helix Dental Implant Recall: Packaging Mismatch Risk (July 13, 2026).
How to tell if you have this one
Check for the product name 'Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm' and catalog number 21-70020. The recall includes items with UDI: 07290108695649 and lot number WO-011320.
Brand
Paltop
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the product name, catalog number, and UDI to confirm if your implant is affected.
Where it went and when
Where it was distributed
Distributed in 10 states and D.C..
Listed by the agency
Not listed
FDA distribution: “The products were distributed to the following US states: CA, DC, FL, GA, MA, MD, NJ, NY, SC, TX, and VA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, District of Columbia, Florida, Georgia, Maryland, Massachusetts, New Jersey, New York, South Carolina, Texas, Virginia.
Recall timeline
FDA terminated this recall 3.1 years 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-0836-2020 (November 18, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0836-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.