🔍 RecallPedia

CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840

Class I - Dangerous
🏥 Medical Devices Recalled: April 24, 2019 Centurion Medical Products Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    2018012450 2018020850 2018062750 2018071250 2018090650 2018101250 2019022550
  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:
Centurion Medical Products Corporation
Reason for Recall:
Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840

Product Codes/Lot Numbers:

2018012450 2018020850 2018062750 2018071250 2018090650 2018101250 2019022550

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0089-2020

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