FDA Drug recall D-0923-2018
Glutathione 200mg/mL Injection w/Pres. (Benzyl Alcohol 1.5% in Sterile Water), 30 mL vial, Rx only, la VITA Compounding Pharmacy, 858.453.2…
- FDA Drug
- Class II
- terminated
- Published 2018-07-25
On 2018-07-25 the FDA classified a Class II recall of Glutathione 200mg/mL Injection w/Pres. (Benzyl Alcohol 1.5% in Sterile Water), 30 mL vial, Rx only, la VITA Compounding Pharmacy, 858.453.2… by La Vita Compounding Pharmacy, citing lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0923-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-06-25 |
| Published | 2018-07-25 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | La Vita Compounding Pharmacy |
| Distribution | CA |
Product
Glutathione 200mg/mL Injection w/Pres. (Benzyl Alcohol 1.5% in Sterile Water), 30 mL vial, Rx only, la VITA Compounding Pharmacy, 858.453.2500
Reason
Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.
Identifiers
| code_info | Lot #: 144326@3, Exp 07/10/2018; 145953@2, Exp 08/05/2018 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0923-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.