FDA Drug recall D-1083-2014
VoLumen Barium Sulfate Suspension (0.1 % w/v, 0.1 ww/w), 450 mL bottle, Rx Only
- FDA Drug
- Class III
- terminated
- Published 2014-02-19
On 2014-02-19 the FDA classified a Class III recall of VoLumen Barium Sulfate Suspension (0.1 % w/v, 0.1 ww/w), 450 mL bottle, Rx Only by Bracco Diagnostics, citing failed Stability Testing: This product is below specification for preservative content.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1083-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-12-16 |
| Published | 2014-02-19 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Bracco Diagnostics |
| Distribution | US |
Product
VoLumen Barium Sulfate Suspension (0.1 % w/v, 0.1 ww/w), 450 mL bottle, Rx Only. Manufactured by E-Z-EM Canada Inc. a subsidiary or E-Z-EM, Inc. Lake Success, NY 11042. NDC 32909-945-03.
Reason
Failed Stability Testing: This product is below specification for preservative content.
Identifiers
| code_info | Lot #: 67603, Expiry: 2/2014 |
|---|
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-1083-2014%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.