Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GLUTATHIONE L REDUCED 100MG/ML (2ML NEBVL) INHALATION Recalled by Pharmacy Innovations Due to Lack of Assurance of Sterility: FDA inspection revealed...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Pharmacy Innovations directly.
Affected Products
GLUTATHIONE L REDUCED 100MG/ML (2ML NEBVL) INHALATION; GLUTATHIONE L REDUCED 200MG/ML (1ML NEBVL) INHALATION; GLUTATHIONE L REDUCED 220MG/ML (30ML VIAL) INJECTABLE; GLUTATHIONE L REDUCED 500MG/ML (1ML VIAL) INJECTABLE; GLUTATHIONE L REDUCED 500MG/ML (2ML VIAL) INJECTABLE; GLUTATHIONE L REDUCED-PF- 200MG/ML (2ML VIAL) INJECTABLE, Rx Only, Pharmacy Innovations, 2936 W 17th St., Erie, PA.
Quantity: N/A
Why Was This Recalled?
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Pharmacy Innovations
Pharmacy Innovations has 59 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report