Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SPECTRUM Pump Recalled by Baxter Healthcare Corp. Due to One Service Technician may not have correctly serviced...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Baxter Healthcare Corp. directly.
Affected Products
SPECTRUM Pump, Model No. 35700BAX. Intended to be used for the controlled administration of intravenous fluids.
Quantity: USA: 56 units, Canada: 2 units
Why Was This Recalled?
One Service Technician may not have correctly serviced specific Sigma Spectrum Infusion Pumps according to established procedures during the time period of 5/5/2014 through 6/3/2014.
Where Was This Sold?
Worldwide Distribution -- USA and Canada.
About Baxter Healthcare Corp.
Baxter Healthcare Corp. has 126 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report