Recalls for Ketorolac Tromethamine Injection, USP, 30mg/mL single-dose vials

Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of Three Lots of Ketorolac Tromethamine Injection, USP, 30mg/Ml Due to Labeling the Product With the Incorrect Expiration Date
10/03/2014 Food Recall

Sagent Pharmaceuticals, Inc. today announced the voluntary nationwide recall of three lots of Ketorolac Tromethamine Injection, USP, 30mg/mL single-dose vials (NDC numbers 25021-701-01 and 25021-701-02) manufactured by Cadila Healthcare Limited and distributed by Sagent. Sagent has initiated this voluntary recall of Ketorolac Tromethamine Injection, USP, 30mg/mL to the user level due to labeling the product with the incorrect expiration date.

  • Company:
    Sagent Pharmaceuticals
  • Problem
    Due to labeling the product with the incorrect expiration date/The labeled expiration date is longer than the known stability of the product.