Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ascorbic Acid 500 MG/ML Inj. Recalled by RemedyRepack Inc. Due to Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
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 RemedyRepack Inc. directly.
Affected Products
Ascorbic Acid 500 MG/ML Inj., Qty: 50 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0431-16
Quantity: 1 Vial
Why Was This Recalled?
Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About RemedyRepack Inc.
RemedyRepack Inc. has 60 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report