Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DEXAMETHASONE 16MG/ML (3ML VIAL) INJECTABLE 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
DEXAMETHASONE 16MG/ML (3ML VIAL) INJECTABLE; DEXAMETHASONE 24MG/ML INJECTABLE; DEXAMETHASONE-PF- 0.1% (1ML DROPPER) OPH SOLUTION, 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