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
Spectrum IQ Infusion Pump Recall Summary Baxter Healthcare Corporation is recalling Spectrum IQ Infusion Pumps (Model 3570009) because they were distributed without complete testing, specifically missing occlusion alarm testing. This Class II recall affects infusion pumps that may not properly detect and alert when tubing becomes blocked. The recall applies to pumps that were released to customers without full safety verification procedures.
- Recalling firm
- 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
- Category
- consumer product recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-01-13
- Status
- Open, Classified
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ea20be66-cde2-45b0-836b-179338763d4b