Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967

Class I - Dangerous
🏥 Medical Devices Recalled: February 9, 2024 Preat Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Model Number: 9000967 UDI-DI code: 00842092165867 Lot Numbers: 235650, 234294, 233667, 233885, 233439, and 231489
  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:
Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967

Product Codes/Lot Numbers:

Model Number: 9000967 UDI-DI code: 00842092165867 Lot Numbers: 235650, 234294, 233667, 233885, 233439, and 231489

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1321-2024

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 →