Glutathione 200 mg/mL Injectable — Class II drug recall D-0335-2015
Terminated recall by Right Value Drug Stores, Inc., reported 2015-01-14, distributed in KS, MO, TX. Incorrect Product Formulation: An incorrect gas was used to remove the oxygen from the vial.
| Recall number | D-0335-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Right Value Drug Stores, Inc., Hurst, TX, United States |
| Recall initiated | 2014-12-12 |
| Classified | 2015-01-08 |
| Reported by FDA | 2015-01-14 |
| Terminated | 2016-11-23 |
| Distributed | KS, MO, TX |
Product
Glutathione 200 mg/mL Injectable, packaged in a) 5 mL MDV (multiple dose vials), b) 30 mL MDV (multiple dose vials), and c) 100 mL MDV (multiple dose vials), Rx only, Carie Boyd's Prescription Shop, 122 Grapevine Highway, Hurst, TX 76054, (817) 282-9376.
Reason for recall
Incorrect Product Formulation: An incorrect gas was used to remove the oxygen from the vial.
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-0335-2015. 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.