Acella Pharmaceuticals, LLC recalls NAPROXEN ORAL SUSPENSION, USP, 125 mg/5mL, Rx only, 16fl oz (473 mL) bottles, Distributed by: Acella Pharmaceuticals, L…
- Recall date
- April 20, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0523-2026
- FDA classification
- Class II
- Brand / firm
- Acella Pharmaceuticals, LLC
- Sold / distributed
- Nationwide
Why it was recalled
Chemical contamination; presence of lead and lithium above specification
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
NAPROXEN ORAL SUSPENSION, USP, 125 mg/5mL, Rx only, 16fl oz (473 mL) bottles, Distributed by: Acella Pharmaceuticals, LLC, Alpharetta, GA 30005, Made in Canada NDC 42192-619-16
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