Glutathione 100 mg/mL Injectable — Class II drug recall D-1019-2013
Terminated recall by Creative Compounds, reported 2013-09-18, distributed in OR, WA. Glutathione 100 mg/mL injectable human drug is recalled due to Out Of Specification results or potential bacte
| Recall number | D-1019-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Creative Compounds, Wilsonville, OR, United States |
| Recall initiated | 2013-08-23 |
| Classified | 2013-09-10 |
| Reported by FDA | 2013-09-18 |
| Terminated | 2013-09-16 |
| Distributed | OR, WA |
| Quantity | 16 vials |
| Reason classes | microbial contamination, specification failure |
| Expiration dates | 2013-10-13 |
Product
Glutathione 100 mg/mL Injectable, 100mL Vial, Use as Directed, RX, Creative Compounds, Wilsonville, OR 97070.
Reason for recall
Glutathione 100 mg/mL injectable human drug is recalled due to Out Of Specification results or potential bacterial contamination and it was reported as passing by a contract laboratory.
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-1019-2013. 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.