🔍 RecallPedia

Monterey AL Implant Inserter; 22mm; Catalog 48019140.

Class I - Dangerous
🏥 Medical Devices Recalled: February 28, 2025 Stryker Spine Implants & Prosthetics

What Should You Do?

  1. Check if you have this product:
    Catalog 48019140; UDI-DI: 07613327501124; Lot Number: 231640;
  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:
Stryker Spine
Reason for Recall:
Potential for the gold unlock button to separate from the inserter.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Monterey AL Implant Inserter; 22mm; Catalog 48019140.

Product Codes/Lot Numbers:

Catalog 48019140; UDI-DI: 07613327501124; Lot Number: 231640;

Distribution:

Distributed in: CA, CO, FL, GA, IL, MA, NE, NH, NY, OK, PA, TX, UT

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1491-2025

Related Recalls