Approximately 467 Plum A+ Single Channel Infusion Pumps intended for veterinary use are being recalled because the internal regulator closer may not seat correctly. This defect can prevent the pump from automatically stopping the flow of fluids or medication when the pump door is opened. If the manual clamp is not closed before opening the cassette door, a patient could receive an unintended and unrestricted flow of medication.
The incorrect seating of the regulator closer fails to engage the safety mechanism that stops fluid flow. This can cause the rapid, uncontrolled administration of fluids or drugs, which poses a serious risk of overdose or injury to animals being treated.
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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