Hikma Injectables USA ketamine inj 50 mg per 1 mL recall — FDA D-0173-2025
Lack of Assurance of Sterility: The tamper-evident seal on several of the syringes are not attached upon receipt of shipment.
Overview of recall records associated with Hikma Injectables USA Inc, including dates, categories and classifications where available.
Classification mix: Class II: 2.
Lack of Assurance of Sterility: The tamper-evident seal on several of the syringes are not attached upon receipt of shipment.
Lack of Assurance of Sterility: The tamper-evident seal on several of the syringes are not attached upon receipt of shipment.
This page summarizes recall records in which the official source identifies Hikma Injectables USA Inc as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.