ALTERA Spacer ALTERA Spacer, 10x36, 8-12mm, 8¿

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Part #: 1124.1211; Lot # / UDI #: BAX103VE / (01)00889095069877(10)BAX103VE; BAX109ME / (01)00889095069877(10)BAX109ME; BAX203PE / (01)00889095069877(10)BAX203PE; BAX315BE / (01)00889095069877(10)BAX315BE; BAX359ME / (01)00889095069877(10)BAX359ME; BAX412WE / (01)00889095069877(10)BAX412WE
  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:
Globus Medical, Inc.
Reason for Recall:
Specific lots of ALTERA¿ implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

ALTERA Spacer ALTERA Spacer, 10x36, 8-12mm, 8¿

Product Codes/Lot Numbers:

Part #: 1124.1211; Lot # / UDI #: BAX103VE / (01)00889095069877(10)BAX103VE; BAX109ME / (01)00889095069877(10)BAX109ME; BAX203PE / (01)00889095069877(10)BAX203PE; BAX315BE / (01)00889095069877(10)BAX315BE; BAX359ME / (01)00889095069877(10)BAX359ME; BAX412WE / (01)00889095069877(10)BAX412WE

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2865-2020

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