FDA Drug recall D-0094-2017
5% Dextrose Injection USP, 100mL in a 150 mL PAB container, Rx only, B. Braun Medical Inc
- FDA Drug
- Class I
- terminated
- Published 2016-10-19
On 2016-10-19 the FDA classified a Class I recall of 5% Dextrose Injection USP, 100mL in a 150 mL PAB container, Rx only, B. Braun Medical Inc by B Braun Medical, citing non-Sterility: fungal contamination due to leaking containers.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0094-2017 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2016-03-25 |
| Published | 2016-10-19 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | B Braun Medical |
| Distribution | US |
Product
5% Dextrose Injection USP, 100mL in a 150 mL PAB container, Rx only, B. Braun Medical Inc. Irvine, CA 92614-5895 USA, NDC 00264-1510-32
Reason
Non-Sterility: fungal contamination due to leaking containers.
Identifiers
| code_info | Lot #: J5J706, Exp. 10/31/2016 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0094-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.