🔍 RecallPedia

Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002

Class I - Dangerous
🏥 Medical Devices Recalled: July 27, 2021 Clarus Medical Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Model Numbers 1100-002 and 1100-002 SHORT; Serial Numbers 64139 through 65022
  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:
Clarus Medical, Llc
Reason for Recall:
The sterile barrier seal may be compromised.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002

Product Codes/Lot Numbers:

Model Numbers 1100-002 and 1100-002 SHORT; Serial Numbers 64139 through 65022

Distribution:

Distributed in: US

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2405-2021