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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Monitoring Devices

Baxter Healthcare Corporation: Spectrum IQ Infusion Pumps Recalled for Potential Front Panel Cracks

Agency Publication Date: May 13, 2024
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Summary

Baxter Healthcare Corporation is recalling 9 Spectrum IQ Infusion pumps (Product Code 357009) because there is a potential for cracks to develop on the mount of the front panel. These infusion pumps are used in healthcare settings to deliver fluids such as nutrients and medications into a patient's body in controlled amounts. Consumers should check if their device matches the specific serial numbers listed below and contact the manufacturer for further instructions.

Risk

Cracks on the front panel mount of the infusion pump can compromise the structural integrity of the device, potentially leading to equipment failure or incorrect delivery of fluids. Any malfunction in an infusion pump can result in serious health consequences for patients who rely on precise dosing of medications or fluids.

What You Should Do

  1. Check your device to see if it is a Spectrum IQ Infusion pump with Product Code 357009.
  2. Verify if your device's serial number is among the 9 affected units: 3770692, 3770755, 3770781, 3770816, 3770932, 3771122, 3771364, 3771374, or 3771419.
  3. If you identify an affected device, contact your healthcare provider or the manufacturer, Baxter Healthcare Corporation, at 1-800-422-9837 for further instructions and potential repair or replacement.
  4. Healthcare facilities should follow their internal protocols for managing recalled medical equipment to ensure patient safety.
  5. For additional information, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer instructions

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Spectrum IQ Infusion pump
Model / REF:
357009
UPC Codes:
00085412610900
Lot Numbers:
3770692
3770755
3770781
3770816
3770932
3771122
3771364
3771374
3771419

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94451
Status: Active
Manufacturer: Baxter Healthcare Corporation
Sold By: Direct distribution
Manufactured In: United States
Units Affected: 9 units
Distributed To: Ohio, Wisconsin

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.