Class I · High riskTerminated Initiated Nov 21, 2013 (13 years ago)
Cefazolin for Injection USP and Dextrose Injection USP, 2 g in Duplex, 50 mL Container…
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
Cefazolin for Injection USP and Dextrose Injection USP, 2 g in Duplex, 50 mL Container, Catalog Number 3105-11, Rx Only, B Braun Medical Inc., Irvine CA 92614, NDC 0264-3105-11
Recalling firm
B. Braun Medical Inc
NDC code
0264-3105-11
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1269-2014
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.
Reason Labeling: Label Mix-Up; cartons of Cefazolin for Injection, USP 1 gram were found to contain vials labeled as penicillin G potassium for Injection…