Avantor Performance Materials LLC has recalled 36 bottles of Magnesium Chloride (6-Hydrate, Crystal), which is a bulk active pharmaceutical ingredient (API) used in compounding or manufacturing medications. The recall was initiated because the product was found to be subpotent, meaning it does not meet the required strength or concentration standards. Consumers and facilities who purchased this specific bulk ingredient should contact their supplier or the manufacturer to arrange for its return.
A subpotent drug ingredient may not provide the intended therapeutic effect when used to create medications, which could lead to ineffective treatment for patients relying on the final pharmaceutical product.
Recall #: D-0488-2026
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
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.