FDAFDA · Food and drugs·Recall number D-0577-2018
Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-215-05
Published March 14, 2018 · Recall initiated: February 21, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Stability Specification: OOS low viscosity results discovered during retain testing.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Akorn, Inc.
- Distributor
- Nationwide in the USA
- Lot
- Lot: 011037A
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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