FDAFDA · Food and drugs·Recall number Z-1944-2024
Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 10013072 Tubing set used for delivery of fluids, medication, blood and blood products.
Published June 12, 2024 · Recall initiated: April 18, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Due to infusion set tubing drip chamber becoming detached from the tubing potentially causing delays in treatment, or unintentionally exposing users to harsh infusates.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- BD SWITZERLAND SARL
- Distributor
- Worldwide - US Nationwide distribution in the states of AR, CA, CO, IL, KS, MA, ME, NJ, NY, PA, SD, WA and WI. The country of Canada.
- Lot
- Catalog Number: 10013072 UDI-DI code:07613203021210 Lot Number: 22115368
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Switzerland
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