🔍 RecallPedia

8MM,CADIERE FORCEPS,IS4000 ¿ REF 470049

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: 470049 Part Number: 470049-08 UDI-DI code: 00886874112250 Batch Numbers: K10221218 K10221220 K10230219 K10230226 K10230302 K10230310 K10230316 K10230323 K10230330 K10230405 K10230413 K10230420 K10230601 K10230608 K10230615 K10230706 K10230720 K10230921 K10230928 K10231005 K10231012 K10231109 K10231130 K10240327 K10240404 K10240418 K10240425 K10240502 K10240515 K11230413 K11230420 K11230720 K11231130 K11240502 K11240515
  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,CADIERE FORCEPS,IS4000 ¿ REF 470049

Product Codes/Lot Numbers:

Model Number: 470049 Part Number: 470049-08 UDI-DI code: 00886874112250 Batch Numbers: K10221218 K10221220 K10230219 K10230226 K10230302 K10230310 K10230316 K10230323 K10230330 K10230405 K10230413 K10230420 K10230601 K10230608 K10230615 K10230706 K10230720 K10230921 K10230928 K10231005 K10231012 K10231109 K10231130 K10240327 K10240404 K10240418 K10240425 K10240502 K10240515 K11230413 K11230420 K11230720 K11231130 K11240502 K11240515

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0853-2025

Related Recalls