11" Smallbore Ext Set w/NanoClave, 6-Port NanoClave Manifold, Check Valve, Clamp, Rotating Luer.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Item Number AM6127. a. Lot Number 3379607, UDI Number (01) 1 0887709 08635 4 (17) 211201 (30) 50 (10) 3379607, Expiration Date 12/01/2021; b. Lot Number 3436226, UDI Number (01) 1 0887709 08635 4 (17) 220401 (30) 50 (10) 3436226, Expiration Date 04/01/2022
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
11" Smallbore Ext Set w/NanoClave, 6-Port NanoClave Manifold, Check Valve, Clamp, Rotating Luer.
Product Codes/Lot Numbers:
Item Number AM6127. a. Lot Number 3379607, UDI Number (01) 1 0887709 08635 4 (17) 211201 (30) 50 (10) 3379607, Expiration Date 12/01/2021; b. Lot Number 3436226, UDI Number (01) 1 0887709 08635 4 (17) 220401 (30) 50 (10) 3436226, Expiration Date 04/01/2022
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.govFDA Recall Number: Z-2814-2018
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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.