Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 25021-0701-02 recalled?

Ketorolac Tromethamine · 25 VIAL in 1 CARTON (25021-701-02) / 2 mL in 1 VIAL

Yes — this exact package was recalled

2 FDA recalls name the code 25021-0701-02 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
ketorolac tromethamine
Strength
KETOROLAC TROMETHAMINE 30 mg/mL
Form
Injection, Solution · Intramuscular, Intravenous
Labeler
Sagent Pharmaceuticals
Type
Human Prescription Drug
Product code
25021-0701

Recalls naming this package

Class II · Moderate risk

Ketorolac Tromethamine Injection

Lack of Sterility Assurance: Microbial growth detected during a routine simulation of the manufacturing process, which represents the potential introduction of microorganisms into the products.

Terminated Sterility / contamination Sagent Pharmaceuticals Inc D-1274-2019
Class II · Moderate risk

Ketorolac Tromethamine INJECTION

Incorrect or Missing Lot and/or Exp Date: Ketorolac Tromethamine Injection, is being recalled as a result of labeling the product with the incorrect expiration date.

Terminated Stability / shelf life Sagent Pharmaceuticals Inc NDC 25021-701-01 D-0027-2015

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler