🔍 RecallPedia

8MM,LONG TIP FORCEPS,IS4000 REF 471048

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: 471048 Part Number: 471048-09 UDI-DI code: 00886874115930 Batch Numbers: K10230330 K10230420 K10230515 K10230706 K10230720 K10230810 K10230907 K10230921 K10231005 K10231019 K10231102 K10231123 K10231207 K10240229 K10240314 K10240321 K10240411 K10240418 K10240509 K10240516 K10240718 K10240725 K10240822
  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,LONG TIP FORCEPS,IS4000 REF 471048

Product Codes/Lot Numbers:

Model Number: 471048 Part Number: 471048-09 UDI-DI code: 00886874115930 Batch Numbers: K10230330 K10230420 K10230515 K10230706 K10230720 K10230810 K10230907 K10230921 K10231005 K10231019 K10231102 K10231123 K10231207 K10240229 K10240314 K10240321 K10240411 K10240418 K10240509 K10240516 K10240718 K10240725 K10240822

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0872-2025

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