Elekta Solutions AB is recalling four systems featuring the MOSAIQ Oncology Information System (Software Builds 3.1.3, 3.2.1, 3.2.2, and 3.2.3.0). The recall was initiated because of a software defect that occurs when appending a care plan containing one or more wave medication orders; in these cases, the frequency and timing of the orders may not match the schedule intended by the physician. Consumers should contact the manufacturer or their distributor immediately to arrange for a software correction or update.
If medication orders are scheduled with the wrong frequency or timing, patients may receive treatments incorrectly, which can compromise the safety and effectiveness of their oncology care.
Recall affects 4 systems that contain the software builds mentioned. Detailed UDI strings include version suffixes: 3.1.3.0 (01)07340201500026(10)3.1.3.0, etc.
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
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