🔍 RecallPedia

Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210

Class I - Dangerous
🏥 Medical Devices Recalled: August 8, 2023 FX SHOULDER Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI-DI: 03701037309551, Lot: U0191
  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:
FX SHOULDER
Reason for Recall:
Centered glenosphere box may contain an eccentric glenosphere.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210

Product Codes/Lot Numbers:

UDI-DI: 03701037309551, Lot: U0191

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0843-2024