Class II · Moderate risk
Fluconazole Injection
Lack of assurance of sterility: customer complaints received for the presence of leaks.
National Drug Code
Is NDC 0338-6046-48 recalled?
Fluconazole · 10 BAG in 1 CARTON (0338-6046-48) / 100 mL in 1 BAG
Yes — this exact package was recalled
3 FDA recalls name the code 0338-6046-48 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
- Fluconazole
- Strength
- FLUCONAZOLE 200 mg/100mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Baxter Healthcare Company
- Type
- Human Prescription Drug
- Product code
- 0338-6046
Recalls naming this package
Class II · Moderate risk
Fluconazole Injection
Lack of Assurance of Sterility: confirmed customer complaints of leaking bags.
Class II · Moderate risk
Fluconazole Injection
Lack of Assurance of Sterility: Complaints of leaks due to an incomplete seal at the bag seam.
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
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.