Reported Jul 23, 2025 · Ongoing
Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2
Baxter Healthcare Corporation
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
Baxter SIGMA Spectrum Infusion Pump V8Model Number 35700BAX2
- Lot codes and dates
- UDI-DI00085412498683
- Serial Numbers
2006307205209120937652095360210430221192362141815202592520676992094483209554121052382119436214340620342972074097209458020963512105769213548221436842051591209065820952022096856211894021379762156201
- Amount recalled
- 28 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Stop using this product now
Certain Spectrum infusion pumps may have an incorrect version of software.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Baxter Healthcare Corporation recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.