FDA Drug recall D-0335-2015
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 (mul…
- FDA Drug
- Class II
- terminated
- Published 2015-01-14
On 2015-01-14 the FDA classified a Class II recall of 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 (mul… by Right Value Drug Stores, citing incorrect Product Formulation: An incorrect gas was used to remove the oxygen from the vial.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0335-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-12-12 |
| Published | 2015-01-14 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Right Value Drug Stores |
| Distribution | 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
Incorrect Product Formulation: An incorrect gas was used to remove the oxygen from the vial.
Identifiers
| code_info | Lot #: 11142014@5, 10142014@17, 11032014@13, 08262014@6, 09162014@6, 06272014@12, 08052014@5, 07222014@18, 07222014@3, 06262014@11, 06182014@3 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0335-2015%22
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