FDAFDA · Food and drugs·Recall number Z-1810-2024
Spectrum IQ Infusion pump, Product Code 357009
Published May 22, 2024 · Recall initiated: April 9, 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
There is a potential for cracks on the mount of the front panel of the device.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Baxter Healthcare Corporation
- Distributor
- US Nationwide distribution in the states of Ohio, Wisconsin.
- Lot
- UDI/DI 00085412610900, Serial Numbers: 3770692, 3770755, 3770781, 3770816, 3770932, 3771122, 3771364, 3771374, 3771419
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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