Hospira Inc. is recalling approximately 449 Hospira Plum XLD Single Channel Infusion Pumps intended for veterinary use. The recall was initiated because these pumps may fail to sound an audible alarm when the audio level is set to the 'low' setting. This defect means that veterinary staff may not be alerted to critical pump conditions, such as occlusions or delivery errors, which could interrupt treatment for animals. These specific pumps were distributed nationwide and are identified by list number 12570.
If the audible alarm fails to sound while on a low volume setting, caregivers may not be alerted to infusion problems or device failures. This can lead to a delay or interruption in the delivery of life-sustaining medications or fluids to animal patients.
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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