Class II · Moderate risk
Sterile Water for Injection USP
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
National Drug Code
Is NDC 0264-7385-60 recalled?
Sterile Water · 4 CONTAINER in 1 CASE (0264-7385-60) / 3000 mL in 1 CONTAINER
Yes — this exact package was recalled
2 FDA recalls name the code 0264-7385-60 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.
2 of these recalls are still ongoing.
- Active ingredient
- Water
- Strength
- WATER 1 mL/mL
- Form
- Injection · Intravenous
- Labeler
- B. Braun Medical Inc.
- Type
- Human Prescription Drug
- Product code
- 0264-7385
Recalls naming this package
Class II · Moderate risk
Sterile Water for Injection USP
Lack of Assurance of Sterility- Potential for fluid leakage from the port due to port misalignment.
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.