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Products intended or expected to be sterile were prepared, packed, or held under unsanitary conditions.Essential Extras: Tailstorm initiated a voluntary recall of the drug bevacizumab in November 2024 due to concerns over sterility.Types of Products Made: Pre-filled sterile injectable products and repackaged products, including single-dose liquid injectable vialsLink: FDA Warning LetterRead the warning letter for a complete description of violations

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