Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts
Class II · Moderate risk Terminated Initiated Sep 21, 2016 (10 years ago)

Glutathione 200 mg/mL Injectable

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility

Cause type: Sterility / contamination

A product that must be sterile could not be assured sterile, or was contaminated. A top reason for injectables, eye drops and IV products - loss of sterility assurance can lead to serious infections. All sterility / contamination recalls.

What was recalled

Glutathione 200 mg/mL Injectable, 30 mL vial, Compounded by Wells Pharmacy, Ocala, FL

Drug: Glutathione

Recalling firm
Wells Pharmacy Network LLC
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0361-2017 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Glutathione recalls

See all
Class I · High risk

Glutathione 200 mg/mL

Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.

Ongoing Microbial contamination Optimal Balance Pharmacy D-0851-2026
Class I · High risk

Glutathione

Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.

Ongoing Microbial contamination Victory Medical Center Pharmacy D-0772-2026

Other recalls by Wells Pharmacy Network LLC

All 2016 recalls