Tailstorm Health INC is recalling 76,300 vials of various injectable medications, including Lidocaine, Bupivacaine, and Ketamine, that were compounded by Medivant Healthcare. The recall was initiated following an FDA inspection that identified concerns regarding the sterile manufacturing process. These products are used in medical offices for anesthesia and nerve blocks, and the company has voluntarily initiated the recall to prevent potential patient harm.
Injectable drugs that are not properly sterilized can introduce bacteria or other contaminants directly into a patient's body. This poses a significant risk of causing serious or life-threatening infections, such as sepsis.
For Infiltration & Nerve Block, Including Caudal & Epidural Use.
For Nerve Block, Caudal & Epidural Anesthesia Only. Warning: Contains Sulfites.
For IM Use or Slow IV Use.
For IM or Slow IV Use.
For Infiltration & Nerve Block, Including Caudal & Epidural Use.
For Infiltration & Nerve Block, Including Caudal & Epidural Use.
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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