CLASS II Drug recall · Reported 14 Jan 2015 · FDA Enforcement Report
Glutathione 200 mg/mL Injectable recalled by Right Value Drug Stores
Right Value Drug Stores is recalling Glutathione 200 mg/mL Injectable, distributed in Kansas, Missouri, Texas. The recall was initiated on 12 Dec 2014 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0335-2015
- FDA event ID
- 70003
- Recalling firm
- Right Value Drug Stores, Hurst, TX
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 12 Dec 2014
- FDA classified
- 8 Jan 2015
- Reported
- 14 Jan 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Packaging Defects
- Drug class
- Injectable & IV Drugs
Timeline
| 12 Dec 2014 | Recall initiated by company | |
| 8 Jan 2015 | Classified by FDA | +27 days |
| 14 Jan 2015 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Incorrect Product Formulation: An incorrect gas was used to remove the oxygen from the vial.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
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.
Where it was distributed
KS, MO, and TX.
Questions about this recall
Why was it recalled?
Incorrect Product Formulation: An incorrect gas was used to remove the oxygen from the vial.
Which lots are affected?
Lot #: 11142014@5, 10142014@17, 11032014@13, 08262014@6, 09162014@6, 06272014@12, 08052014@5, 07222014@18, 07222014@3, 06262014@11, 06182014@3
Where was it sold?
KS, MO, and TX.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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Other Glutathione recalls
All 41| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Glutathione 200 mg/mL sterile multidose vial recalled | Optimal Balance Pharmacy | Sterility | Nationwide |
| Drug | CLASS II | Glutathione Magnesium for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Glutathione 200mg/ml, a)-vial, b)-vial, Refrigerate recalled | TMC Acquisition | Sterility | Nationwide |
| Drug | CLASS II | Glutathione 200mg/mL Preservative Free, Injectable-vial recalled | TMC Acquisition | Sterility | Nationwide |
| Drug | CLASS II | Glutathione 200mg/ML Mdv recalled by First Royal Care Co. LLC | First Royal Care Co. LLC | Sterility | 7 states |