Hospira Inc. is recalling 467 Plum A+ Infusion Systems due to a software issue that causes an 'E321' error code. This error occurs when the device is plugged into AC power but fails to fully recharge its battery within eight hours. When this error triggers during an infusion, the pump will automatically stop delivering fluids or medication, which can lead to a serious delay or interruption in treatment. This recall affects various serial numbers under List Number 60529 that were distributed nationwide.
The software triggers a complete stop of fluid delivery if it detects a battery charging delay, even while the unit is plugged into a wall outlet. This interruption can cause critical delays in the administration of life-sustaining parenteral, enteral, or epidural medications.
Correction for E321 software error
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.
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 · Raw API Response