Neodent GM X 6mm Engaging Titanium Base, REF: 9007162

Class I - Dangerous
🏥 Medical Devices Recalled: February 21, 2023 Preat Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI: 00842092161326, Lots: 211891 and 211912
  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:
Preat Corp
Reason for Recall:
Engaging titanium base contains a dimensional condition that allows vertical movement of the titanium base after the prosthetic screw is torqued to the recommended value, which if undetected and installed on the implant, may lead to abutment/screw fracture, which could result in the abutment/screw/crown being ingested by the patient.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Neodent GM X 6mm Engaging Titanium Base, REF: 9007162

Product Codes/Lot Numbers:

UDI: 00842092161326, Lots: 211891 and 211912

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1285-2023

Related Recalls

Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant.

Apr 2, 2025 Implants & Prosthetics Nationwide View Details →