Hospira Inc. is recalling 467 units of the Plum A+ Infusion System because a component called the fluid shield diaphragm may be out of specification. This defect can cause the pump to trigger 'Door Open while pumping' (N250) or 'Unrecognizable Cassette' (N100) alarms during setup or infusion. These alarms can lead to an unexpected delay or interruption in the delivery of critical fluids, such as medications, nutrients, or blood, to patients.
If the fluid shield diaphragm fails, it triggers audible and visual alarms that stop the infusion process. This interruption can result in a delay of therapy, which may have serious health consequences depending on the patient's condition and the medication being delivered.
Equipment inspection and potential repair
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