112" (284 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter, Hand Pump, 3 Clave¿, Rotating Luer, 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 - DangerousWhat Should You Do?
- Check if you have this product: Item Number Z1440, Lot Number 69-334-SJ, 70-212-SL, 70-913-SL, 70-937-SJ, 71-660-Y1, 72-392-HE, 72-620-HE, 72-905-HE, 73-158-HE, 73-389-HE, 73-625-HE, 73-995-HE, 74-006-JW, 74-307-JW, 74-453-JW, 74-714-JW, 75-430-JW, 75-656-JW, 75-834-JW
- 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, 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:
112" (284 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter, Hand Pump, 3 Clave¿, Rotating Luer, 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 Z1440, Lot Number 69-334-SJ, 70-212-SL, 70-913-SL, 70-937-SJ, 71-660-Y1, 72-392-HE, 72-620-HE, 72-905-HE, 73-158-HE, 73-389-HE, 73-625-HE, 73-995-HE, 74-006-JW, 74-307-JW, 74-453-JW, 74-714-JW, 75-430-JW, 75-656-JW, 75-834-JW
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2640-2018
Related Recalls
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
Port weld of drug transfer device may separate or break during use and potentially result in a leak.