Baxter Sigma Spectrum Infusion System recall
Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX
Why was Baxter Sigma Spectrum Infusion System recalled?
There is the potential for missing motor mounting screws, which may have occurred during the servicing process.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI 00085412091570, Serial Numbers: 704198, 728888, 751492, 758399, 758614, 761662, 763197, 766291, 772611, 773302, 775486, 778837, 785425, 793453, 795240, 798065, 814485, 818850, 826637, 850214, 850854, 851500, 854157, 855803, 863354, 870307, 873114, 876483, 877014, 877102, 889153, 896292, 900181, 906422, 907176, 912242, 913562, 927864, 938265, 958176, 962828, 963975, 965158, 974676, 981605, 982459, 984154, 986132, 986634, 989053, 993087, 994417, 994842, 995538, 997153, 1006359, 1011058, 1013925, 1014064, 1014529, 1014856, 1017150, 1017546, 1018229, 1018703, 1024109
- Product
- Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 66 units
- Distribution
- US: Nationwide
- Recall date
- March 12, 2025
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)