Baxter Healthcare Corporation Spectrum IQ Infusion pump, Product Code 357009 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Spectrum IQ Infusion pump, Product Code 357009
Brand
Baxter Healthcare Corporation
Lot Codes / Batch Numbers
UDI/DI 00085412610900, Serial Numbers: 3770692, 3770755, 3770781, 3770816, 3770932, 3771122, 3771364, 3771374, 3771419
Products Sold
UDI/DI 00085412610900, Serial Numbers: 3770692, 3770755, 3770781, 3770816, 3770932, 3771122, 3771364, 3771374, 3771419
Baxter Healthcare Corporation is recalling Spectrum IQ Infusion pump, Product Code 357009 due to There is a potential for cracks on the mount of the front panel of the device.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is a potential for cracks on the mount of the front panel of the device.
Recommended Action
Per FDA guidance
Baxter notified its consignees of the issue and requested an on-site inspection of the affected units on 04/09/2024 via telephone.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026