FDAFDA · Food and drugs·Recall number Z-1775-2024
Baxter Spectrum IQ Infusion Pump, Product Code 3570009
Published May 15, 2024 · Recall initiated: March 20, 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
One device was improperly performed testing prior to release from a Service Center.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Baxter Healthcare Corporation
- Distributor
- US Nationwide distribution in the state of Massachusetts.
- Lot
- UDI/DI 00085412610900, Serial Number 3540772
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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