Pharmacy Innovations recalls glutathione L reduced inhalation and injectable products due to FDA-identified insanitary conditions at manufacturing facility. Products may contain contaminants that could cause infection.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling several glutathione L reduced products, including inhalation and injectable forms, because FDA inspections found unsanitary conditions at their facility. This could mean the products contain contaminants that might cause infections if used.
FDA inspections found unsanitary conditions at Pharmacy Innovations' manufacturing facility. This could lead to products containing contaminants that might cause infections if used. The hazard is related to the facility's cleanliness during production.
People who purchased or have Pharmacy Innovations' glutathione L reduced inhalation or injectable products. Those with medical conditions requiring these products may be at higher risk.
Check for products labeled 'GLUTATHIONE L REDUCED 100MG/ML (2ML NEBVL) INHALATION', 'GLUTATHIONE L REDUCED 200MG/ML (1ML NEBVL) INHALATION', or similar injectable forms from Pharmacy Innovations. Products were sold between October 2022 and November 2022.
Look for the product names listed in the recall notice to confirm if your product is affected.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility, which could lead to products containing contaminants that might cause infections.
The affected products include glutathione L reduced inhalation and injectable forms such as 100mg/ml (2ml nebulizer), 200mg/ml (1ml nebulizer), and 500mg/ml (1ml or 2ml vials).
Check the product labels for the specific names listed in the recall notice and verify the manufacturer is Pharmacy Innovations.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0210-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0210-2023 from Pharmacy Innovations. 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.
