🔍 RecallPedia

EndoTool SubQ (Versions 1.7.1, 1.7.4, 1.7.5)

Class I - Dangerous
🏥 Medical Devices Recalled: October 1, 2019 Monarch Medical Technologies Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    versions: v 1.7.1, 1.7.4, 1.7.5
  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:
Monarch Medical Technologies
Reason for Recall:
Product was distributed prior to approval or clearance from FDA.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

EndoTool SubQ (Versions 1.7.1, 1.7.4, 1.7.5)

Product Codes/Lot Numbers:

versions: v 1.7.1, 1.7.4, 1.7.5

Distribution:

Distributed in: SC, IL, IN, CA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0354-2020

Related Recalls