Brilliant Blue G BBG — Class II drug recall D-1055-2016
Terminated recall by Vital Care Compounder, reported 2016-07-06, distributed in MS. Lack of Assurance of Sterility: Aluminum crimps do not fully seal the rubber stopper to the vials.
| Recall number | D-1055-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vital Care Compounder, Hattiesburg, MS, United States |
| Recall initiated | 2015-06-10 |
| Classified | 2016-06-28 |
| Reported by FDA | 2016-07-06 |
| Terminated | 2016-11-17 |
| Distributed | MS |
| Quantity | 9 vials |
| Reason classes | sterility, packaging |
| Lot numbers | 395575 |
| Expiration dates | 2016-07-27 |
Product
Brilliant Blue G BBG, 0.025%, Sterile Injection, 0.5 mL Single Dose Vial, Vital Care Compounder, Hattiesburg, MS
Reason for recall
Lack of Assurance of Sterility: Aluminum crimps do not fully seal the rubber stopper to the vials.
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-1055-2016. 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.