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On July 9, 2025, a recall was initiated due to a detected issue with a product identified as Acepromazine maleate. The incident was reported in the United States of America and classified under the category of product recall. The primary concern associated with this recall is that the product does not meet specified potency requirements.
The U.S. Food and Drug Administration has been informed about this incident, which raises important safety considerations regarding the efficacy of the affected product. The recall process aims to ensure that any products failing to meet established potency specifications are appropriately addressed to maintain safety standards and regulatory compliance.
As the situation develops, further information may be provided by relevant authorities to ensure that stakeholders are informed about the implications of the recall. Ensuring product quality and safety is crucial in the pharmaceutical sector, and the detection of such discrepancies highlights the importance of rigorous quality control measures.
Individuals with concerns regarding Acepromazine maleate or the recall process are encouraged to consult official sources for guidance and updates.
- Incident: Product does not meet potency specifications has been detected in Acepromazine maleate.
- Date: 2025-07-09
- Product: Acepromazine maleate
- Market: Available to SGS Digicomply users only. Explore the platform (for enterprises, no individual plans)
- Origin of issue: United States of America
- Hazard: Available to SGS Digicomply users only. Explore the platform (for enterprises, no individual plans)
- Incident Category: Recall
- Hazard Category: null
- Source: U.S. Food and Drug Administration
For more detailed information about this and other similar incidents, with access to filtering options, historical data, and trend analysis, try the SGS Digicomply Food Safety Software.
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