Central Admixture Pharmacy Services, Inc. (CAPS) is voluntarily recalling 233,401 units of various admixture injections including Fentanyl, Hydromorphone, Morphine, and several other medications. These products, distributed in syringes and IV bags, were sold nationwide directly to hospitals, clinics, and surgical centers. The recall was initiated because the company lacks validation data for the sanitization cycles used during production, which means the sterility of the products cannot be fully assured. To date, there have been no reported incidents or injuries related to this issue.
Injectable medications that are not sterile can cause serious infections or life-threatening systemic illnesses when administered to patients. Because these medications are injected directly into the bloodstream or body tissues, any bacterial contamination poses a significant risk to health.
Quantity: 100 syringes
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Quantity: 1,669 syringes
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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
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