Red Mountain Compounding Pharmacy recalls ascorbic/glutathione eye drops (Rx only) due to FDA sterility concerns. All lots within expiry date are affected. Consumers should contact the pharmacy for details.
Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Red Mountain Compounding Pharmacy is recalling ascorbic/glutathione eye drops (Rx only) because FDA inspections found sterility assurance issues. This could lead to infections if the product is not sterile.
The FDA identified sterility assurance problems during inspections. This means the product might not be sterile, increasing infection risk if used.
People with prescriptions for this eye drop solution. Those with compromised immune systems or open wounds may be at higher risk.
Look for the product name 'Ascorbic/Glutathione 1.25/1.25% OPTH SOLN' on the label. It's a prescription-only eye drop solution sold by Red Mountain Compounding Pharmacy.
Reach out to Red Mountain Compounding Pharmacy directly for specific details about the affected product and next steps.
The FDA found sterility assurance concerns, so the product may not be sterile. It's recommended to stop using and contact the pharmacy.
Look for the product name 'Ascorbic/Glutathione 1.25/1.25% OPTH SOLN' on the label. It's a prescription-only eye drop solution sold by Red Mountain Compounding Pharmacy.
Contact Red Mountain Compounding Pharmacy directly for specific details about the affected product and next steps.
We’ve drafted a message you can send Red Mountain Compounding Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0033-2022 — Red Mountain Compounding Pharmacy Red Mountain Compounding Pharmacy Hello, I own a Red Mountain Compounding Pharmacy that is covered by recall D-0033-2022 from Red Mountain Compounding Pharmacy. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.