🔍 RecallPedia

8MM,BLACK DIAMOND MICRO FORCEPS,IS4000 ¿ REF 470033

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: 470033 Part Number: 470033-09 UDI-DI code: 00886874112229 Batch Numbers: K10230219 K10230316 K10230511 K10230615 K10230706 K10230713 K10230824 K10230928 K10231005 K10231109 K10231218 K10240104 K10240229 K10240418 K10240613 Part Number: 470033-11 UDI-DI code: 00886874112229 Batch Number: K10230914
  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,BLACK DIAMOND MICRO FORCEPS,IS4000 ¿ REF 470033

Product Codes/Lot Numbers:

Model Number: 470033 Part Number: 470033-09 UDI-DI code: 00886874112229 Batch Numbers: K10230219 K10230316 K10230511 K10230615 K10230706 K10230713 K10230824 K10230928 K10231005 K10231109 K10231218 K10240104 K10240229 K10240418 K10240613 Part Number: 470033-11 UDI-DI code: 00886874112229 Batch Number: K10230914

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0851-2025

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