E-Z-CAT Dry Barium Sulfate for Suspension — Class III drug recall D-1147-2015
Terminated recall by Bracco Diagnostic Inc, reported 2015-07-01, distributed nationwide. Failed stability specifications:This recall has been initiated due to out of specification results for viscosi
| Recall number | D-1147-2015 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bracco Diagnostic Inc, Monroe Township, NJ, United States |
| Recall initiated | 2015-05-27 |
| Classified | 2015-06-22 |
| Reported by FDA | 2015-07-01 |
| Terminated | 2016-02-19 |
| Distributed | Nationwide (US) |
| Quantity | 1,008 boxes |
| Reason classes | specification failure |
| NDC | 32909-0727-01 |
| Lot numbers | 00513716, 00514712 |
| Expiration dates | 2016-03 |
Product
E-Z-CAT Dry Barium Sulfate for Suspension (2% w/w after mixing), 23 g foil pouches, Rx only, Manufactured by E-Z-EM Canada Inc. a subsidiary of E-Z-EM Inc., Lake Success NY NDC 32909-727-01
Reason for recall
Failed stability specifications:This recall has been initiated due to out of specification results for viscosity.
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-1147-2015. 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.