Reported Mar 12, 2025 · Ongoing
Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX
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 System (V6 Platform), Product Code 35700BAX
- Lot codes and dates
- UDI/DI 00085412091570
- Serial Numbers
66 of 66 codes
70419872888875149275839975861476166276319776629177261177330277548677883778542579345379524079806581448581885082663785021485085485150085415785580386335487030787311487648387701487710288915389629290018190642290717691224291356292786493826595817696282896397596515897467698160598245998415498613298663498905399308799441799484299553899715310063591011058101392510140641014529
- Amount recalled
- 66 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
- Nationwide
Why it was recalled
Stop using this product now
There is the potential for missing motor mounting screws, which may have occurred during the servicing process.
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.
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