🔍 RecallPedia

REF 8420.15.020, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=25mm, STERILE R, 2100099, UDI: (01)08033390018852

Class I - Dangerous
🏥 Medical Devices Recalled: October 1, 2021 Limacorporate S.p.A Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    2103525
  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:
Limacorporate S.p.A
Reason for Recall:
There is a potential that the length of bone screws identified on labeling may not correspond to the actual length of the screw included.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

REF 8420.15.020, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=25mm, STERILE R, 2100099, UDI: (01)08033390018852

Product Codes/Lot Numbers:

2103525

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0159-2022

Related Recalls