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Direct RxFDAMed source confidence · 83%Jul 7, 2026, 7:47 AM UTC · 1d ago

Direct Rx — FDA Class II (D-0617-2026)

Case File

Direct Rx is recalling 263 bottles of their drug due to CGMP deviations. The recall is prompted by the presence of N-nitroso-d. This action affects products distributed from their facility at 94 Worldwide Dr, Georgia.

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Key Points
  • Direct Rx is recalling 263 bottles of their drug.
  • The recall is due to contamination with N-nitroso-d.
  • This action is classified as a Class II recall.
  • Consumers should check their medicine cabinets for this product.
Why This Matters

Consumers who purchased this drug should stop using it and return it. The recall affects 263 bottles due to contamination.

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