10" Smallbore Ext Set w/6-Port NanoClave Manifold, Check Valve, Clamp, Rotating Luer

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Item Number AM6109. a. Lot Number 3373758, UDI Number (01) 1 0887709 07764 2, Expiration Date 12/01/2021; b. Lot Number 3391364, UDI Number (01) 1 0887709 07764 2 (17) 220101 (30) 50 (10) 3391364, Expiration Date 01/01/2022; c. Lot Number 3511445, UDI Number (01) 1 0887709 07764 2 (17) 220801 (30) 50 (10) 3511445, Expiration Date 08/01/2022
  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:
ICU Medical de Mexico, S.A. de C.V.
Reason for Recall:
ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Administration Sets with NanoClave manifold due to the potential to develop a leak or for separation between the female luer and the NanoClave manifold.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

10" Smallbore Ext Set w/6-Port NanoClave Manifold, Check Valve, Clamp, Rotating Luer

Product Codes/Lot Numbers:

Item Number AM6109. a. Lot Number 3373758, UDI Number (01) 1 0887709 07764 2, Expiration Date 12/01/2021; b. Lot Number 3391364, UDI Number (01) 1 0887709 07764 2 (17) 220101 (30) 50 (10) 3391364, Expiration Date 01/01/2022; c. Lot Number 3511445, UDI Number (01) 1 0887709 07764 2 (17) 220801 (30) 50 (10) 3511445, Expiration Date 08/01/2022

Distribution:

Distributed in: US, AZ, MA, NC, OH, TX, VA, WA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2813-2018

Related Recalls

ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Administration Sets with NanoClave manifold due to the potential to develop a leak or for separation between the female luer and the NanoClave manifold.

Mar 1, 2018 Other Medical Devices View Details →

ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Administration Sets with NanoClave manifold due to the potential to develop a leak or for separation between the female luer and the NanoClave manifold.

Mar 1, 2018 Other Medical Devices View Details →