CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.
Reason for recall: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. Distribution: Nationwide in the USA and Canada, Dominican Republic, El Salvador, Honduras, and Qatar. Lot/code info: Lot No.: BNZ-001646, Exp Date: 11/26/2026, Keystone Item No. 03-35119
Official record: FDA (Drug enforcement) ↗
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