The Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
Summary
The FDA issued a Class I for The Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 35700 by Baxter Healthcare Corporation. Reason: A medical device correction is being issued for SIGMA Spectrum Infusion System (V8 Platform) and Spectrum IQ Infusion System with Dose IQ Safety Softw.
Details
Source
Device Recall
External ID
Z-2104-2023
Action Date
2023-07-19
Status
Ongoing
Category
device
Product Description
The Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
Lot/Code Info: UDI/DI 00085412610900, Software Version v9.02.01, All Serial Numbers
Quantity Affected: 19861 units
Reason for Recall
A medical device correction is being issued for SIGMA Spectrum Infusion System (V8 Platform) and Spectrum IQ Infusion System with Dose IQ Safety Software infusion pumps due to an increase in reported false upstream occlusion alarms following upgrades to software versions v8.01.01 and v9.02.01.
Distribution
US Nationwide distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-06-15
Company
Deerfield, IL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 165 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Baxter Healthcare Corporation has 310 FDA actions in our database, including 286 recalls and 24 clearances.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Baxter Healthcare Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Baxter Healthcare Corporation have FDA actions?
Baxter Healthcare Corporation has 310 FDA actions in our database, including 286 recalls and 24 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-2104-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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