Hospira Inc. is recalling 1,168 Plum XL Family infusion pumps because the door roller assembly can break. This device is used to deliver medications, nutrients, and blood products to patients in hospitals and home care settings. If the internal door roller pin breaks, the pump cannot properly lock the medication cassette into position, which may cause the door to stay open or trigger false alarms. Consumers should contact their healthcare provider or the manufacturer to ensure their device is functioning correctly.
A broken door roller pin prevents the device from securing the fluid cassette properly. This failure can cause the infusion to stop unexpectedly, trigger false occlusion alarms, or prevent the device from being closed and started, potentially delaying critical medical treatments.
Device inspection and support
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