Public recall detail

Spectrum Iq Infusion System With Dose Iq Safety Software

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Recall Safety notice
Quick summary

Quick summary: Spectrum Iq Infusion System With Dose Iq Safety Software.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Spectrum Iq Infusion System With Dose Iq Safety Software.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandBaxter Healthcare Corporation
ProductSpectrum Iq Infusion System With Dose Iq Safety Software
IssueMedical devices - Performance
Recall classType II
IdentificationRA-63794

Affected products

ProductSpectrum Iq Infusion System With Dose Iq Safety Software
LotAll lots.
Model3570009
Serial numberAll lots.
DescriptionSpectrum Iq Infusion System With Dose Iq Safety Software

Issue

Baxter is communicating important safety information for Spectrum V8 and Spectrum IQ Infusion Pumps related to potential reduced or non-delivery of medication, in some cases without alerting the user via pump alarm. This may occur as a result of incorrect administration set setup and/or incomplete resolution of upstream occlusion alarms. Recall start date: December 29, 2021.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Health professionals Hospitals
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesPublished by Health Canada
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-63794
Background{}
CompaniesPublished by Health Canada
AudiencesGeneral public Health professionals Hospitals
Source updated2022-01-04

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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