Baxter Healthcare Corporation recalls Brand Name: Spectrum IQ Product Name: Infusion Pump
- Recalling company
- Baxter Healthcare Corporation
- Product
- Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product Description: Infusion Pump, one unit per carton Component: N/A
- Reason
- Pumps were released without full testing being performed, including occlusion alarm testing.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jan 13, 2026
- Reported
- Feb 25, 2026
- Distribution
- States: Ohio Countries: United States
- Status
- Ongoing
- Quantity
- 5
- Lot / codes
- Lot Code: GTIN 00085412610900, Serial Numbers 3815663, 3823468, 3824743, 3825234, and 3825599
- Company location
- Deerfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1368-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1368-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.