FDASeptember 18, 2018device

SPECTRUM IQ INFUSION SYSTEM WITH DOSE IQ SAFETY SOFTWARE, 3570009

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

If an operator attempts to manually program a Basic Infusion for a drug that is not included in the Drug Library using the Basic-Dose Mode, the operator will receive a false hard limit exceeded error, preventing him or her from programming the infusion.

What to do

FDA enforcement status: Terminated

Brands named

baxter healthcarebaxter

UPCs

00085412610900

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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