159" (404 cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, Remv 4-Way Stopcock, 3 Pre-Pierced Ports, Luer Lock, 2 Ext, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use as an adjunct to blood tubing sets or venipuncture devices for needle-free withdrawal of blood.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Item Number Z2902, Lot Number 69-365-SJ, 69-707-SJ, 70-196-SL, 70-400-SL, 70-759-SL, 70-918-SL, 70-952-SJ, 71-189-Y1, 71-562-Y1, 71-669-Y1, 71-861-Y1, 73-604-HE, 73-877-HE, 74-014-JW, 74-320-JW, 74-463-JW, 74-733-JW, 75-262-JW, 75-420-JW, 75-644-JW, 75-846-JW, 76-096-SJ
  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, Inc.
Reason for Recall:
Some devices were labeled as Does not contain DEHP even though the product may contain small amounts of DEHP.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

159" (404 cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, Remv 4-Way Stopcock, 3 Pre-Pierced Ports, Luer Lock, 2 Ext, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use as an adjunct to blood tubing sets or venipuncture devices for needle-free withdrawal of blood.

Product Codes/Lot Numbers:

Item Number Z2902, Lot Number 69-365-SJ, 69-707-SJ, 70-196-SL, 70-400-SL, 70-759-SL, 70-918-SL, 70-952-SJ, 71-189-Y1, 71-562-Y1, 71-669-Y1, 71-861-Y1, 73-604-HE, 73-877-HE, 74-014-JW, 74-320-JW, 74-463-JW, 74-733-JW, 75-262-JW, 75-420-JW, 75-644-JW, 75-846-JW, 76-096-SJ

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2649-2018

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