Hospira Inc. is recalling 467 units of the Plum A+ Infusion System because a component called the door roller assembly can break during use. This mechanical failure can occur when a nurse or caregiver is removing the IV cassette from the pump, potentially leading to unrestricted fluid flow or the over-delivery of medication to the patient. These pumps are multi-function infusion systems used to deliver various fluids and medications in healthcare environments.
If the door roller assembly breaks, the pump may fail to properly regulate fluid delivery when the IV set is removed. This can cause the patient to receive too much medication or fluid too quickly, which poses a serious risk of medical complications or injury.
Manufacturer instruction 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