VoLumen Barium Sulfate Suspension — Class III drug recall D-1083-2014
Terminated recall by Bracco Diagnostics Inc, reported 2014-02-19, distributed nationwide. Failed Stability Testing: This product is below specification for preservative content.
| Recall number | D-1083-2014 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bracco Diagnostics Inc, Monroe Township, NJ, United States |
| Recall initiated | 2013-12-16 |
| Classified | 2014-02-07 |
| Reported by FDA | 2014-02-19 |
| Terminated | 2015-01-23 |
| Distributed | Nationwide (US) |
| Quantity | 54,648 bottles |
| Reason classes | specification failure |
| NDC | 32909-0945-03 |
| Lot numbers | 67603 |
| Expiration dates | 2014-02 |
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 for recall
Failed Stability Testing: This product is below specification for preservative content.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1083-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.