Baxter recalls Spectrum IQ Infusion Pumps (product code 3570009) due to potential medication delivery issues from incorrect setup or unresolved alarms. Affected units have specific serial numbers and GTIN.
There is the potential for reduced or non-delivery of medication, in some cases without alerting the user via pump alarm. This may occur as a result of incorrect administration set setup and/or incomplete resolution of upstream occlusion alarms when using Spectrum V8 and Spectrum IQ infusion pumps.
Baxter is recalling Spectrum IQ Infusion Pumps with product code 3570009 because they might not deliver medication properly, especially if setup is incorrect or alarms aren't fixed. This could lead to medication not being given as intended.
The pumps might not deliver medication correctly if the administration setup is wrong or if upstream occlusion alarms aren't fully resolved. This could cause medication to not be given as intended, especially without the pump alerting the user.
Patients using Baxter Spectrum IQ Infusion Pumps for medication delivery are affected. Those with pumps that have the specific product code or serial numbers listed are most at risk.
Check for the product code 3570009 on the pump or its documentation. Affected units have specific serial numbers and GTIN 00085412610900.
Ensure the administration set is correctly set up and upstream occlusion alarms are fully resolved to prevent medication delivery issues.
Baxter Spectrum IQ Infusion Pumps with product code 3570009.
Check for the product code 3570009 on the pump or its documentation. Affected units have specific serial numbers and GTIN 00085412610900.
Ensure the administration set is correctly set up and upstream occlusion alarms are fully resolved to prevent medication delivery issues.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0529-2022 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0529-2022 from Baxter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
