Ranitidine Hydrochloride Capsules recalled over foreign material
- Recall date
- September 23, 2019
- Source
- U.S. Food & Drug Administration (FDA) — recall announcement
- Official notice title
- Sandoz Inc. recalls Sandoz Inc. — Ranitidine Hydrochloride Capsules
- Brand / firm
- Sandoz Inc., Sandoz Inc.
Why it was recalled
Due to an Elevated Amount of Unexpected Impurity, N-Nitrosodimethylamine (NDMA) — Potential Foreign Material
What was recalled
Ranitidine Hydrochloride Capsules
Read the official recall notice →
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