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Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312

Class I - Dangerous
🏥 Medical Devices Recalled: July 9, 2024 Medtronic Perfusion Systems Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    GTIN 20613994879329, Lot Numbers: 2023090954, 202312C065
  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:
Medtronic Perfusion Systems
Reason for Recall:
During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312

Product Codes/Lot Numbers:

GTIN 20613994879329, Lot Numbers: 2023090954, 202312C065

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-3128-2024

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