Class II · Moderate risk
Ketorolac Tromethamine Injection
Presence of Particulate Matter: Particulate matter identified as glass
National Drug Code
Is NDC 31722-0307-02 recalled?
Ketorolac Tromethamine
Yes — this exact package was recalled
1 FDA recall names the code 31722-0307-02 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.
1 of these recalls is still ongoing.
- Active ingredient
- Ketorolac Tromethamine
- Strength
- KETOROLAC TROMETHAMINE 60 mg/2mL
- Form
- Injection, Solution · Intramuscular, Intravenous
- Labeler
- Camber Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 31722-0307
Recalls naming this package
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
- 31722-0726 Montelukast Sodium 3
- 31722-0713 Pantoprazole Sodium 2
- 31722-0270 See recall 1
- 31722-0513 Simvastatin 1
- 31722-0525 Finasteride 1
- 31722-0530 Torsemide 1
Free recall alerts
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