Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm Catalog Number: 20-70024P

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot Number: W0-008254 UDI: 729010869611020-70024P
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Paltop Advanced Dental Solutions Ltd
Reason for Recall:
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm Catalog Number: 20-70024P

Product Codes/Lot Numbers:

Lot Number: W0-008254 UDI: 729010869611020-70024P

Distribution:

Distributed in: AL, AZ, CA, CO, FL, GA, MA, MD, MO, MT, NJ, NM, NY, OH, SC, VA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0019-2020

Related Recalls

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.

Jul 26, 2021 Implants & Prosthetics Nationwide View 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.

Jul 26, 2021 Implants & Prosthetics Nationwide View 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.

Jul 26, 2021 Implants & Prosthetics Nationwide View Details →