Class II · Moderate risk Terminated
Cefepime for Injection
Reason Lack of Assurance of Sterility
Cefepime for Injections USP and Dextrose Injection USP
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
What was recalled
Cefepime for Injections USP and Dextrose Injection USP, 1 g in Duplex, 50 mL Container, Catalog Number 3193-11, For IV Use Only, Single Dose, Sterile, Rx Only, B Braun Medical Inc., Irvine CA 92614-5895, NDC 0264-3193-11
- Recalling firm
- B. Braun Medical Inc
- NDC code
- 0264-3193-11
- Origin
- CA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1267-2014
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Cefepime recalls
See all
Class II · Moderate risk Terminated
Cefepime for Injection
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Cefepime for Injection
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Cefepime for Injection
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Cefepime for Injection
Reason Lack of Assurance of Sterility
Get an alert if your medication is recalled
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.