🔍 RecallPedia

8MM,MEGA SUTURECUT ND,IS4000¿ REF 470309

Class I - Dangerous
🏥 Medical Devices Recalled: December 19, 2024 Intuitive Surgical Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Model Number: 470309 Part Number: 470309-15 UDI-DI code: 00886874112434 Batch Numbers: K10230217 Model Number: 470309 Part Number: 470309-17 UDI-DI code: 00886874112410 Batch Numbers: K10230302
  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:
Intuitive Surgical, Inc.
Reason for Recall:
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

8MM,MEGA SUTURECUT ND,IS4000¿ REF 470309

Product Codes/Lot Numbers:

Model Number: 470309 Part Number: 470309-15 UDI-DI code: 00886874112434 Batch Numbers: K10230217 Model Number: 470309 Part Number: 470309-17 UDI-DI code: 00886874112410 Batch Numbers: K10230302

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0865-2025

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