🔍 RecallPedia

Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A1 C17/5 -ceramic for dental use, intended for IPS e.max ZirCAD presintered yttrium oxide-stabilized zirconium oxide blocks for the CAD/CAM technology Product Number: 686193

Class I - Dangerous
🏥 Medical Devices Recalled: April 13, 2020 Ivoclar Vivadent AG Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Number: Y48711
  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:
Ivoclar Vivadent AG
Reason for Recall:
Restorations crack during the sintering process.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A1 C17/5 -ceramic for dental use, intended for IPS e.max ZirCAD presintered yttrium oxide-stabilized zirconium oxide blocks for the CAD/CAM technology Product Number: 686193

Product Codes/Lot Numbers:

Lot Number: Y48711

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1837-2020

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